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ProSeal™ Add Mixture Device (ADRx)

Pharmacists and nurses can now expand their capabilities without limitations in bag types or hospital compounding and infusion procedures. Whether in the pharmacy or on the ward, from vial to any bag, ProSeal™ ADRx Devices offer a more advanced and simplified approach to medication transfer.

All Round Medication Transfer

ADRx Devices simplify the transfer of various medications, including powdered (lyophilized agents) and liquid drugs, from vials to flexible bags, eliminating the need for syringes and needles.

Effortless Process

By connecting the flexible bag to the vial using the ProSeal™ ADRX device, inverting it, and gently squeezing the bag, the vial's pressure increases as air is introduced. Releasing the pressure on the bag allows medication from the vial to be transferred seamlessly into the final container. This allows healthcare professionals and patients to experience a smooth medication transfer.

Versatility and Ease of Use

ProSeal™ ADRx Devices set new standards in versatility and ease of use, allowing medication transfer into any medication bag through both outlet and inlet ports.

Video: ProSeal™ Add Mixture Device (ADRx)
ProSeal CSTD

COMPLIANCE

INTERNATIONAL REGULATORY STANDARDS

European regulatory bodies, including the European Medicines Agency (EMA) and national authorities, are actively engaged in developing and implementing comprehensive regulations and standards for CSTDs. These standards are designed to ensure the safety, efficacy, and quality of CSTDs across the European market. The harmonization of regulatory requirements promotes consistent and standardized use of CSTDs in diverse healthcare settings.


NIOSH REQUIREMENTS

PRoSeal™ CSTDs meet the NIOSH requirements for closed system transfer devices, mechanically preventing the transfer of environmental contaminants and the escape of hazardous drugs or vapor concentrations. For instance, ProSeal™– ToxiSeal Vial Adaptors, are equipped with an external balloon, in addition to a 0.1 micron sterile filter and activated carbon filters.


PHARMACEUTICAL SAFETY STANDARDS

ProSeal™ CSTDs are FDA ONB & FPA code cleared and compliant with USP<797> and USP<800> standards, demonstrating their commitment to pharmaceutical safety regulations.

TESTS

PROVEN MICROBIAL INGRESS PREVENTION

ProSeal™ CSTDs have been rigorously tested and confirmed to prevent microbial ingress for at least 168 hours after 10 activations, ensuring long lasting effectiveness.

ERGONOMICS

USER-FRIENDLY PUSH/PULL ACTION

ProSeal™ Devices feature a quick and simple Push/Pull action, eliminating the need for repetitive rotation and reducing the risk of RSI-type injuries (Repetitive Strain Injuries).


OPTIMIZATION

COST EFFECTIVE & EFFICIENT

Beyond safety, the design of ProSeal™ CSTDs enables efficient manufacturability, resulting in competitive pricing.

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