TWIST-OFF ZERO (Patent Pending)

Spike port with interlocking fastening to the bag tube

The semi-rigid components inserted to close the tubes of bags containing sterile solutions, called Twist-offs, must satisfy the hermetic sealing requirements of a primary pharmaceutical packaging. For this reason, these components must be welded, glued or blocked on the tube through steam sterilization process.
Twist-off ZERO, thanks to its patented geometry, guarantees a validated hermetic closure after its insertion into the bag tube, without the need for further gluing, welding, or thermal sterilization process.
Twist-off ZERO is compliant to the ISO 3826-1 regarding the appropriate distance of the internal membrane for the spike to assure ad adequate hermetic insulation when inserted.
Twist-off ZERO is a patented product available in different PVC FREE materials, suitable for PVC and PVC FREE tubes.

Advantages

  • ZERO need for additional operations
  • ZERO risk of fluid leakage (especially during and after aseptic production processes).
  • ZERO need for thermal sterilization process.
  • ZEROrisk of fluid leakage (especially during and after aseptic production processes).
  • ISO 3826-1 compliant.
  • Available in different PVC FREE materials.
  • Ssuitable for PVC and PVC FREE tubes.

NIP® – “Needleless Injection Point”

Needlefree connectors

Hermetic closure needlefree injection point

Every day, healthcare workers are exposed to dangerous pathogens through contaminated needles. In response to these critical issues, Haemopharm has developed NIP® a needlefree connector, in accordance with FDA regulations and market tendencies, that are moving towards this kind of systems which are more secure to caregivers and to patients.

Advantages

  • NIP® revolutionizes the needlefree connections providing a hermetic closure for powders and liquids in sterile containers, with no risk of contamination.
  • It can be used to access the bag with a luer connector, without the needle, avoiding accidental needle sticks, improving safety for patients and caregivers
  • As soon as the luer is removed, NIP® hermetically closes again preventing the back flow effect.
  • Thanks to the hermetic closure, NIP® can substitute injection ports and breakable cones and can be used for I.V. set connection, without spike.

NIV® – “Needleless Injection Vial” (Patented)

Needlefree connectors

Hermetic closure needlefree vial stopper

Many medications are stored in vials and extracted with a syringe, including antibiotics and chemotherapy drugs.
The rubber stopper on medication vials protects the contents from outside contamination, and must be penetrated to allow access to the medication.
When drawing medication from a rubber-topped vial, it is essential that the proper procedures are followed, to prevent contamination and ensure the correct dosage.

Advantages

  • Needlefree device, in compliance with the most advanced policies
  • Possibility to be custom designed
  • Minimizes foam formation during drug reconstitution, assuring the correct drug dose to the patient, avoiding medication waste and overfilling
  • Mechanically and microbiologically closed system during and after multi-use, and therefore hermetically closed, avoiding contamination of the vial’s contents
  • Reduces aerosol and leaks caused by pressurization when accessing the vial
  • Innovative material

CSTD REFill Kit (Patented)

Intravenous Therapy
Urology - Oncology
Oncology
Drug Reconstitution

Ready-to-use system for reconstitution and administration to the patient of one or more drug vials.


CSTD CSTD Refill® KIT, is the latest generation of systems for the reconstitution and administration of drugs, which consists of the combination of a dedicated bag and one or more Refill connectors for each vial to be reconstituted.

In the common clinical practice of drug reconstitution, healthcare professionals perform a multi-step procedure that exposes them to serious risks resulting from the use of syringes with needles and the potential release of cytotoxic drugs in the form of drops, vapor or aerosols.

In accordance with the safety guidelines for healthcare personnel, CSTD Refill® KIT introduces an innovative solution on the market: a single product for the reconstitution of multiple drug vials and for the administration to the patient which ensures the closed system and guarantees the safety of operators and patients.

CSTD Refill® KIT, is composed of one or more Refill connectors (one for each vial to be reconstituted) and a dedicated sterile bag (for I.V administration / Instillation) , empty (to be filled at the hospital pharmacy) or pre-filled with solvent. This combination creates a ready-to-use, safe and convenient system.

SAFE RECONSTITUTION WITHOUT NEEDLES. CSTD REFill® KIT is designed in accordance with international needle-free policies: this eliminates the risk of accidental needle sticks, which could cause serious damage to the operators’ health, especially in the presence of cytotoxic and dangerous drugs.

SAFETY OF THE CLOSED CIRCUIT. During the reconstitution operations there is an important risk of leakage of dangerous drugs in the form of drops, particles or aerosol into the surrounding environment. This involves a serious danger to the health of healthcare professionals who perform the drug reconstitution. The closed system of CSTD CSTD REFill® KIT prevents the risk of drug leakage avoiding internal and external contamination.

ALL IN ONE & READY TO USE. The combination of the dedicated bag and the REFill connector allows the operator to prepare, reconstitute and administer the drug to the patient, with a ready for use device, that does not require additional materials: everything needed for the reconstitution and administration of the drug is contained within the same device.

MULTIVIAL RECONSTITUTION. CSTD REFill® KIT is a device designed for the reconstitution of multiple vials within the same bag, ready for administration, using a dedicated REFill for each vial to be reconstituted.

HOME THERAPY. The safety and ease of use features of CSTD REFill® KIT make it perfectly suitable for the preparation and admi­nistration of drugs at home.

CONVENIENCE AND SUSTAINABILITY. The CSTD REFill® KIT system eliminates the need for additional materials and accessories (e.g. needle syringes typically used for drug reconstitution): in this way, consumables and waste are reduced – and therefore also the environmental impact, health procedures are facilitated and speeded up, and logistics and warehouse management are optimized, allowing for better cost control.


SIV® CSTD (Patented)

Intravenous Therapy
Oncology
Drug Reconstitution

“Sterile Injection Vial”. Connessione sterile in sistema chiuso

The preparation of cytotoxic drugs requires a delicate and complex multi-step procedure, to be performed with extreme care. Ina typical reconstitution process, the drug contained in the vial is solubilized and transferred into the bag for administration to the patient, with the use of a syringe with a needle. At each step, the contact surfaces must be disinfected to avoid microbial contamination of the drug. These operations require the utmost caution, in order to not compromise sterility and avoid damage to the health of the operator and patient. The procedure is performed by healthcare personnel in a controlled environment in compliance with the strictest hygiene and safety standards such as, for example, under a laminar flow hood in the pharmacy departments of hospital facilities.

SIV® CSTD is a patented closed transfer device that allows the sterile connection between the vial containing a drug to be reconstituted and a bag with solvent.

The SIV® CSTD System consists of a connector and a dedicated vial stopper, suitable for all standard sized drug vials. No modification is required in the capping system of the pharmaceutical manufacturing process.

In compliance with NIOSH recommendations SIV® CSTD allows operators to perform a sterile operation in an uncontrolled environment, thanks to the patented connection between the stopper and the connector. This feature speeds up and simplifies the logistics of healthcare facilities, guaranteeing the safety of operators and patients.

STERILE CONNECTION With SIV® CSTD the drug vial connects to the bag in sterile conditions with a simple handling, even in a NON-controlled environment, such as, for example, the hospital ward. The patented SIV® system prevents any microbial contamination, without the need for manual sanitization with disinfectant, required with common CSTDs on the market.

EASY TO USE SIV® CSTD simplifies the reconstitution procedure: the entire operation can be performed directly in the administration bag, in a single step and with a single device, minimizing the risks and the possibilities of error.

SAFE RECONSTITUTION WITHOUT NEEDLES SIV® CSTD is designed in accordance with international needle-free policies: this eliminates the risk of accidental needle sticks, which could cause serious damage to the operators’ health, especially in the presence of cytotoxic and dangerous drugs.

VIAL STOPPER IN INNOVATIVE MATERIAL The stopper of SIV® CSTD system is produced in an innovative material and with a patented geometry that allows the connector to connect the vial stably and hermetically without the risk of detachment of particles from the cap.

SAFETY OF THE CLOSED CIRCUIT Durante le operazioni di ricostituzione vi è un importante rischio di fuoriuscita di farmaci pericolosi sotto forma di gocce, particolato o aerosol nell’ambiente circostante. Questo comporta un serio pericolo per la salute degli operatori sanitari che effettuano la ricostituzione del farmaco. Grazie al sistema chiuso convalidato, SIV® CSTD evita le possibili contaminazioni dall’ambiente esterno e previene il rischio di perdite di farmaco, come prescritto dalle raccomandazioni NIOSH in materia di sicurezza degli operatori sanitari.

ALL IN ONE & READY TO USE LThe combination of the dedicated bag and SIV® CSTD allows to prepare, reconstitute and administer the drug to the patient, with a single ready-to-use device.The system simplifies and speeds up the operations performed by healthcare personnel.

HOME THERAPY The safety and ease of use of SIV® CSTD make it suitable for the preparation and administration of drugs at home.

CONVENIENCE AND SUSTAINABILITY The possibility of performing all the reconstitution and administration operations using a single device, without additional consumables (syringes, gauze, disinfectant, and more), speeds up and simplifies the logistics and warehouse management of healthcare facilities, reducing consumables and waste, and therefore the environmental impact.

Flexible bags

A wide and diversified production with very high specialization

A widely consolidated know-how and continuous research and innovation allow Haemopharm to produce different types of bags with a high quality standard.

  • PVC / PVC free
  • Single / multi chamber
  • Empty / Filled
  • Customized volume available
  • sterilized / non sterilized
  • Provided with last generation proprietary needlefree connectors

Customization service

In order to meet the specific needs of our customers, our bags can be customized in terms of materials, volume, single or multi-compartment, and configuration.

Innovative and high performance materials

The company can offer cutting-edge materials of the highest quality (in terms of container-content interaction, barrier properties, etc …) suitable for the production of bags and components for the pharmaceutical and medical sector, studying the most suitable solution for each project, to ensure the best preservation and stability of the drug.

Proprietary Machines and molds for PVC and PVC-free bags

Thanks to a high-profile engineering know-how and a large and well-equipped internal workshop, Haemopharm is able to manage the entire production cycle, from the construction of customized machines and molds, to the creation of prototypes up to the production of finished products.

Compliance with medical and pharmaceutical industry standards

All production activities and related procedures are verified and certified by accredited bodies and client companies through periodic audits. The manufacturing processes are carried out under Clean Room conditions, in compliance with international standards UNI EN ISO 14644, UNI EN ISO 14698.
The quality system is ISO 9001 and ISO 13485 certified.

Total quality: advanced online monitoring systems

Haemopharm implemented a pioneering online parametric and inline camera control driven by Artificial Intelligence that allows the 100% inspection of the products. The proprietary software, dedicated to the monitoring of the process and all the production steps, guarantees top-level product quality.

Fillchoice® Smart

Urology - Oncology
Oncology
Drug Reconstitution

Bag for drug reconstitution and vesical instillation with double connectors

The FILLCHOICE® bag, created by Haemopharm’s research and development, guarantees reconstitution also in association of antiblastic drugs in absolute safety and simplicity, thanks to its patented closed circuit system.
The bag can contain a basic infusional solution (solvent) with the volume and formulation requested for the reconstitution.

Main advantages:

  • Closed circuit system during all preparation, reconstitution and infusion operations to the patient, physical and microbiological tests performed by Haemopharm’s Laboratory
  • Possibility of dosing the drug
  • No filters, which are potential cause of drug particulate leak by aerosol effect, and the access of microorganisms
  • Handling of the pressure during the use, guaranteed by the special connector
  • Simple use and a significant reduction of the handling operations
  • No drug aerosol nor particulate leakage outside of the system
  • No needles
  • Drug evidence during the infusion session
  • Cost control

“FillChoice®: Bag for reconstitution and administration of medications” – Download the brochure.

FillChoice® room

Drug Reconstitution

System for drug reconstitution and pharmacy compounding

Fillchoice® Room is an innovative system for drug reconstitution and pharmacy compounding that provides both the vial and the solvent in one single closed package and maintains sterile conditions when connecting the vial and the solvent.
Fillchoice® Room allows to replace the multistep procedure of standard practice and to make the drug reconstitution and compounding pharmacy directly in the bag.

Main advantages

  • TOTAL SAFETY. Fillchoice® Room is not only a closed system but it guarantees 100% isolation: isolation of the drug from external environment and contamination, and isolation of the pharmacist and nurses from the dangerous drug, with no harms in case of leakages, aerosol or accidental break of the vial as everything remains inside the bag with no possibility to exit. Safety is increased by the direct sterile connection vial-bag: Fillchoice® room is the first system that connects the vial and the bag in sterile conditions.

  • EVIDENCE OF THE DRUG IN SITU. As the packaging is completely transparent, the operators perfectly know what’s inside the bag as they can see the vial, the label on the vial (wich contains important data, such as the name of the drug, the quantity, the concentration, the expiry date, etc.). This way there are no problems of unreadable datas and this minimizes medical errors and favours the correct match therapy-patient. Furthermore, Fillchoice® room system contains the precise amount of diluent and drug and guarantees the complete emptying of the vial content, improving dosing accuracy, so that the patient receives the correct dose of the drug.

  • READY TO USE. Using Fillchoice® room there is no need of the hospital pharmacy and the multi-step procedure to make the reconstitution because the vial and the drug are already in the same package and the reconstitution can be easily performed directly in the ward, next to patients bed. Fillchoice® room is also ready to hang for making the infusion to the patient from the same bag where the drug has been reconstituted, saving time and work for the pharmacist and the nurses. It is also important to underline an added value of the Fillchoice® room system as this is perfectly in compliance with the home-care therapies: in most instances, reconstituted drugs are administered in non-clinical settings (typically at home) by patients or caregivers who are not trained health care Professionals. Fillchoice® room is totally safe, very easy to use, with no harms for the user and then suitable also for the non-professionals.

  • NO NEED TO MODIFY THE STANDARDS. The main players are the same used in standard practice: the vial and the bag.
    There is no need for special regulatory and the system can be easily adjusted for several drugs.

  • CUSTOMIZATION. Fillchoice® Room is available for every kind of drug and solvent, any vial size and any solvent volume. There is also the possibility to customize the bag with multiple connectors for multiple vials if a particular compounding is needed (this could be very useful for some antibiotics) and the system remains completely the same: sterile connection vial-bag, one single package, 100% isolation, ready to use. Fillchoice® room can also be provided with different bag material, for special requests of compatibility with drugs or solvent.

  • SUSTAINABILITY. Thanks to its configuration and method of use, Fillchoice® room allows the complete emptying of the vial, even if the drug forms a layer of foam. This means that the patient receives the correct amount of drug and that there is less waste of the active principle: no drug stays unused and thrown away in the vial as it is totally returned to the bag and infused to the patient. For the same reason Fillchoice® room also helps in limiting the overfill of the vial performed by many Pharmaceutical manufacturers (up to 35 percent). Furthermore, there a lot of saved costs for the solvent that is already inside the bag, for the Consumables and disposables that are not needed any more, for the Pharmacist work and time, for the Hospital Pharmacy equipment management and for the logistics: it’s easier to manage one single product instead of multiple products for a multi-step procedure.

FillChoice®

Oncology
Drug Reconstitution

Drug reconstitution bag

The FILLCHOICE® bag, created by Haemopharm’s research and development, allows the reconstitution and intravenous administration of drugs in absolute safety and simplicity, thanks to its patented closed circuit system.
The bag can contain a basic infusional solution (solvent) with the volume and formulation requested for the reconstitution.

Main advantages:

  • Closed circuit system during all preparation, reconstitution and infusion operations to the patient, physical and microbiological tests performed by Haemopharm’s Laboratory
  • Possibility of dosing the drug
  • No filters, which are potential cause of drug particulate leak by aerosol effect, and the access of microorganisms
  • Handling of the pressure during the use, guaranteed by the special connector
  • Simple use and a significant reduction of the handling operations
  • No drug aerosol nor particulate leakage outside of the system
  • No needles
  • Drug evidence during the infusion session
  • Cost control

“FillChoice®: Bag for reconstitution and administration of medications” – Download the brochure.

BI-Bag Line

Drug Reconstitution

Double bag for drug reconstitution

Two-compartment bag for anaesthetic therapy, for transfer and mixing operations, ready to use.

Stemchoice®

Blood & Cell Therapy

Stem cells collection bags

STEMCHOICE® is a double safety bag for cryopreservation of stem cells , made in speciale material for a better resistance in long term conservation in liquid nitrogen. All cryobags go through different testing methods, one by one, both in pre and post production phase. A quality label is applied on the finished product as guarantee of its conformity to the testing results.

The finished product is in compliance with the internal and external quality standards and every production batch release is provided with a Declaration of Conformity and a Production Control report.The Bags, the overwrapping and each individual component belong to a unique project that turns the product user-friendly. Moreover, the bag special design perfectly fits the majority of the existing bag holders.

The special needle-free connector guarantees the safety of the operator and reduces the risk of contamination.The material has the most innovative formulation of EVA, the welding is performed with the most advanced technologies and the components have been chosen in order to guarantee the highest safety and to minimize the risk of contamination.
The blister is made of medical grade paper and disinfectable plastic film, containing the bag and its overwrap.
This simplifies and improves working in sterile conditions.

STEMCHOICE® bags are available in different sizes, depending on the application.

For more information visit www.advatis.com

Tissuechoice®

Blood & Cell Therapy

Bags for cryopreservation of tissues

TISSUECHOICE® is a cryobag dedicated to the cryopreservation of different tissues. It has been developed through an accurate research of materials and components: the material is the most innovative formulation of EVA, the weldings are performed with the most advanced technologies and the connectors have been chosen in order to guarantee the highest safety and to minimize the risk of contamination.

The bag special design has been developed to specifically respond to our customers’ needs and to make the product user-friendly during each step of the manipulation. Moreover, this shape perfectly fits the majority of the existing bag holders. All cryobags go through different testing methods, one by one, both in pre and post production phase. A quality label is applied on the finished product as guarantee of its conformity to the testing results. The finished product is in compliance with the internal and external quality standards and every production batch release is provided with a Declaration of Conformity and a Production Control report.

TISSUECHOICE® is available in different sizes, depending on the kind of application.

For more information visit www.advatis.com

Adipochoice®

Blood & Cell Therapy

Bags for cryopreservation of adipose tissue

ADIPOCHOICE® is the line of bags born from a new project dedicated to the preservation of autologous adipose tissue which, after being extracted and cleaned up, is stored in liquid nitrogen, to then be thawed and reused in cosmetic and reconstructive surgery.

The bag is equipped with special patented connectors, which enable an easy outflow of the adipose tissue that is generally difficult to manipulate due to its special consistency.

For more information visit www.advatis.com

Haemoclean

Dyalisis

Double bag for priming

Bag for extracorporeal circuit rinsing in Haemodialysis.

FKG System

Dyalisis

Double bag for CAPD

Double bag system for Peritoneal Dialysis.

HFS

Dyalisis

Haemofiltration double bag

Available with different hemofiltration formulation.

“CRRT Treatments with citrate” – Download the brochure.

Citrachoice

Dyalisis

Citrate bag for CRRT treatment

CitraChoice is a bag for regional citrate anticoagulation (RCA) for CRRT treatment. Anticoagulation with citrate, which seems to be clinically more interesting in the CRRT techniques with hematic dilution, does not reach the patient’s blood circulation, preventing from clotting, and lowering the amount of ionized calcium, brought to balance in the patient through a continuous infusion of CaCl.

The dialyzers suitable for this therapy must be equipped with the fourth pump. Those currently on the market are:

  • Bellco
  • Hospal/Gambro
  • Fresenius
  • Edwards

“CRRT Treatments with citrate” – Download the brochure.

Alimenta Parenteral

Clinical Nutrition

Sterile bag for parenteral nutrition manufactured with innovative material

Alimenta is the brand line of parenteral nutrition bags manufactured with an innovative material that extremely improves the TPN bag features.

Features

  • Transparency: Alimenta transparent film allows an easy inspection of the solution contained in the bag
  • PH stability: contrary to EVA which could release acetate and lower the pH, any PH variation occurs using Alimenta film
  • O2 permeability: Alimenta film provides a high Oxygen barrier, therefore prevents any oxidation of the solution
  • Sealing technology: bags available in multi-chamber configuration (two, three, four, …) with peel-seal technology
  • Volumes: from 150 to 3500 mL, other volumes on request
  • Design: standard or custom made

iRestore (CE marked)

Ophtalmology

Corneal graft containment solutions

iRestore solutions are synthetic media for corneal storage. The special formulations consist of a mixture of salts, aminoacids, vitamins, nutrients and preservative agents which are suitable for the physiological preservation of corneal tissues. It is well known that highly viable corneal endothelium is fundamental for a successful transplantation. iRestore solutions are enriched with an osmotic agent identified by PAOLO GOBBI FRATTINI R&D department, which avoids tissue edema formation and provide more stable formulations. All the solutions also contain phenol red indicator which allows a rapid visualization of pH variations.

PAOLO GOBBI FRATTINI production process takes advantage of a cutting-edge technique which ensures high qualitative standards.
All solutions are terminally sterilized by filtration (0.22 μm) into a positive pressure isolator. This real closed system guarantees an aseptic environment which few companies in the ophthalmic industry are able to provide.
Corneal explants can be preserved in appropriate media both at physiological temperature (organ culture method) and at 4°C (storage in hypothermic condition).

The iRestore solutions are divided into three categories according to their purpose:

Culture: Sterile liquid for the preservation of corneal tissues up to 30 days (CE marked).

Conservation: Sterile liquid for the preservation of the corneal tissues in hypothermia up to 14 days (CE marked).

Transport: Sterile liquid for deturgescence and transport at room temperature of the corneal tissue, up to 5 days (CE marked).

“Corneal graft containment solutions” – Download the brochure.

iWash

Ophtalmology

Poly-saline solution dispenser

iWash is designed for ocular irrigation during surgical procedures involving the perfusion of the eye.
The physiological pH and the osmotic pressure minimize the trauma of the surgery and protect the corneal tissue, preventing the dehydration, while the transparency and the refraction index of the solution allow a clear view of the surgical procedure.

iodiopharm

Ophtalmology

5% Povidone-Iodine solution dispenser

Iodiopharm is designed for the disinfection of the ophthalmic operating field.
Thanks to its special configuration, it allows the direct and uniform distribution of the product, with no need of pledget or gauzes.

InfusiONcology

Oncology

Infusion set for oncology

InfusiONcology is a line of infusion sets designed specifically for oncology, due to the choice of materials and components. The line can be realized in PVC DEHP-free material or in completely PVC FREE material, both characterized by a certified degree of photosensitivity and therefore light protection.
The components have been selected thanks to a close collaboration with Specialized Italian oncology centers, in order to meet the specific requirements of those who handle anticancer drugs daily.

Features

  • PVC DEHP FREE/ PVC FREE amber photosensitive material: allows a safer use with the most light-sensitive drugs. InfusiONcology is the first line of infusion sets with a certified degree of photosensitivity.
  • Needlefree Connectors: increase operator safety when handling dangerous drugs. The luer access allows the user to connect a luer lock syringe and begin therapy only after locking the syringe on the connector, without any risk of medication leakage.
  • Check valves: allow to infuse the anticancer drug with no error or re-inhalation possibility once the drug was injected
  • ensures no air bubbles or accidental release of the drug
  • Perforator: ergonomic design for easy grip, small size to allow the simultaneous use of two drifters on bag or bottle
  • Inviolable Closing: maximum protection and inability to disconnect

Technical Specifications

  • Certified degree of amber photosensitive tubes and drip chambers, made in PVC DEHP FREE / PVC FREE
  • All the materials are USP class VI
  • Various possible configurations and custom service available in order to meet the needs of the customer

Infusion set bag

Oncology

Bag assembled with infusion set, totally made in PVC-FREE material

The closed circuit ensures the maximum safety for both patients and operators in the handling of dangerous drugs such as antitumorals.

Sano3

Ozone Therapy

Kit for major autohemo infusion with ozone

Sano3 is the First CE marked, patented, complete kit for Major Autohemo Infusion with Ozone.
400 ml bag with transfusion sets, sterile.

Features

  • First complete system authorized by the National Institute of Health (CE specific to the Major Autohemo infusion)
  • Bag for collecting and processing blood without phthalates (plasticizers)
  • Bag for collecting and processing blood inert to ozone (particle detachment)
  • No needles except for the one dedicated to patient withdrawal (removal of accidental punctures with relative risk of infection)
  • Needlefree Connections (ensure hermetic sealing when disconnected from the syringe
  • Absence of clots and gas embolus (SANO3 allows the performance of all the operations necessary for the treatment of Major Autohemo Infusion without risk of blood clots and embolus

For more information visit: www.sanotre.com

“Ozone kit for therapy for major autohemo infusion” – Download the brochure.

washOut

Wound Care

Ergonomic bag for the washing of critical wounds

Features

  • Injection point for adding active principles to the irrigation solution
  • Ergonomic shape of the bag which facilitates the controlled compression for the correct washing pressure on the wound
  • Special patented connector, blade flow, for precise cleaning of the wound
  • Sterile
  • CE marked
  • Volume: 150 ml

Bag Access

Injection Sites

Injection sites

Port Plug

Port plug

Twist-Off bag port, PP TPE

Twist-Off Bag Port, PP TPE

Twist-Off bag port, PVC

Twist-Off bag port, PVC

Vial stopper, PC-PP

Vial stopper, PC-PP

Injection t-port, PC

Injection T-port, PC

Twist off port, E.V.A.

Twist off port, E.V.A.

Breakable cone, female, with cap

Breakable cone, female, with cap

Breakable cone, male, with injection site

Breakable cone, male, with injection site

Drug Reconstitution

Breakable vial adapter

Breakable vial adapter

Breakable vial adapter

Breakable vial adapter

Breakable vial adapter

Breakable vial adapter

Breakable cone for 6x8 mm tube

Breakable cone for 6×8 tube

Components for urology

Barbed and stepped tube reducer with break-off tip and cap

Barbed and stepped tube reducer with break-off tip and cap

Breakable cone, male, with injection site

Breakable cone, male, with injection site

Components for dialysis

Capd connection - Periglass

Capd connection – Periglass®

Capd connection - Periglass Plus®

Capd connection – Periglass Plus®

Capd bag connector

Capd bag connector

Capd set connector

Capd set connector

Capd titanium joint connector

Capd titanium joint connector

Joint connector

Joint connector

Y tubing connector

Y tubing connector

Tubing connector

Tubing connector

FK10

FK10

Patients set connector

Patients set connector

Components for clinical nutrition

Bag handle

Bag handle

In-line flow indicator

In-line flow indicator

Female luer lock connector with cap

Female luer lock connector with cap

Female luer lock connector with cap, non-standard size

Male luer lock connector with cap

General components

Tube reducer

Tube reducer

Pinch clamps

Pinch clamps

Washing components

Smart fluid dispenser with cap

Smart fluid dispenser with cap

Patents

Developed by RENZO GOBBI FRATTINI

1976

Automatic machine for the manufacturing of medical empty bags

Automatic machine for the manufacturing of infusion sets

1982
1984

Intravenous flow regulation system

Machine for the automatic production and packing of infusion sets

(registered under the name Paolo Gobbi Frattini)

1991

Developed by PAOLO GOBBI FRATTINI

1995

PERIGLASS

Sterile environment connection device for CAPD catheter

SHARPBAG®

Bag for drug reconstitution

1996
1999

Connection device for CAPD catheter

HFLINE

Double bag for hemofiltration

2003
2007

SANO3

Kit for oxygen-ozone therapy

WASHOUT

Device for wound washing

2008
2011

NIP®

Needlefree connector


BREATHCHOICE

Double bag for lactose intolerance breath test


FILLCHOICE® DOSE

Bag for dosed drug reconstitution

FILLCHOICE® SMART

Three-way bag for drug reconstitution


NIV®

Perforable hermetic needlefree closure for Vial

2012
2013

Bag-system for liquids

FILLCHOICE® ROOM

System for drug reconstitution


“Method for treating blood cells before separation”

2014
2015

ADIPOCHOICE® SMART

System for adipose tissue treatment


FILLCHOICE® ROOM, and its sterilization method

System for adipose tissue treatment

FILLCHOICE® ROOM DOSE

System for dosed drug reconstitution


SIV®

System for sterile connection

2016
2013

Bag-system for liquids

FILLCHOICE® ROOM

System for drug reconstitution


“Method for treating blood cells before separation”

2014
2015

ADIPOCHOICE® SMART

System for adipose tissue treatment


FILLCHOICE® ROOM and its sterilization method

FILLCHOICE® ROOM DOSE

System for dosed drug reconstitution


SIV®

System for sterile connection

2016
2018

NIP MALE

Male needle free connector


i-Safer

Sterile drop dispenser

“Luer Vial adapter”


REFILL

Vial connector for multivial drug reconstitution systems


Twist.off ZERO

Spike port with interlocking fastening system

2020
2021

“Bag for containment and irrigation of a solution for washing and disinfection of dental surgical field”

Trademarks

1993

UROPOKET®

Registration n. 00685903


PRIMINGLINE®

Registration n. 674438

PERILINE®

Registration n. MI95C 007726

1995
1996

SHARPBAG®

Registration n. M216C 009280

HAEMOPHARM®

Registration n. 003460805

2003
2010

FILLCHOICE®

Registration EU n. 009099615


FILLCHOICE®

Registration USA n. 3977292

TISSUECHOICE®

Registration EU n. 010123602
by Paolo Gobbi Frattini and Medigas Italia S.R.L.


STEMCHOICE®

Registration EU n. 010123644
by Paolo Gobbi Frattini and Medigas Italia S.R.L.


NIP®

Registration USA EU n. 010485118
Registration USA n.4267010

2011
2012

NIV®

Registration EU n. 010957587
Registration USA n. 4500243

INFUSIONCOLOGY®

Registration n. 012399358

2013
2014

SAFE2®

Registration EU n. 1205983
Registration USA n. 4639158

ADVATIS®

Registration n. MI2015C000167
by Paolo Gobbi Frattini and Medigas Italia S.R.L.


ADIPOCHOICE®

Registration EU n. 013922208
by Haemopharm and Medigas Italia S.R.L.


CORDCHOICE®

Registration EU n. 013922174
by Haemopharm and Medigas Italia S.R.L.

2015
2016

ADIPOCHOICE®

Registration USA n. 4888307
by Haemopharm and Medigas Italia S.R.L.


CORDCHOICE®

Registration USA n. 4888306
by Haemopharm and Medigas Italia S.R.L.

FILLCHOICE®

International Registration IR n. 1543440
by Paolo Gobbi Frattini and ADIENNE Pharma & Biotech SA


FILLCHOICE®

Registration HONG-KONG n. 305312934
by Paolo Gobbi Frattini and ADIENNE Pharma & Biotech SA


FILLCHOICE®

Registration TAIWAN n. 02137734
by Paolo Gobbi Frattini and ADIENNE Pharma & Biotech SA

2020