EXPECT NOTHING LESS
ProSeal™
Closed System Transfer Devices
FROM VIAL TO PATIENT //
Reduce risk of exposure to hazardous drugs
EXTENSIVE RANGE OF VIAL ADAPTERS
DRY DISCONNECTION BETWEEN COMPONENTS
PREVENTION OF MICROBIAL INGRESS
ALL COMPONENTS DMA COMPATIBLE
REGULATORY COMPLIANT
FEATURES
PRESSURE EQUALISATION
The ProSeal™ Vial Adapter facilitates equalisation of pressure between the vial and the syringe. This pressure equalisation prevents the escape of fine aerosols into the environment, thereby protecting health care professionals and patients from exposure to hazardous drugs. The ProSeal™ Vial Adapter utilises both a filter and an expandable balloon to capture any vapour completely within the device.
DRY DISCONNECTION
PREVENTION OF MICROBIAL INGRESS
Dry disconnection of components of a CSTD are necessary to prevent droplet exposure of hazardous drugs. All components of ProSeal™ CSTD’s incorporate dual membrane technology, thus achieving 100% dry disconnection after fluid transfers.
A CSTD should prevent the ingress of any contaminants to the system. This should be true during the preparation of and storage of hazardous drugs. ProSeal™ CSTD components are proven to prevent microbial ingress for at least 7 days.
DMA COMPATIBILITY
REGULATORY COMPLIANT
Several antineoplastic agents contain a solvent DMA (N,N-Dimethylacetamide) that is incompatible with polycarbonate plastics in an undiluted form. For example Busulfan requires a dilution when used in many CSTD devices. All Proseal™ CSTD components are made of DMA compatible materials.
The ProSeal™ CSTD is compliant with NIOSH standards, has ONB code with FDA and complies with USP<797> and USP<800>.
ProSeal™ Product Range
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