Vial Adapters

One piercing spike with two lumens:

• One for transfer of drug/solution between the drug vial and a syringe
• Second for enabling pressure equilibrium of the vial by introducing air that has passed through a 0.2 micron hydrophobic air filter into the vial.
• Vial adapters are 510(k) cleared by the United States Food and Drug Administration and carries the CE mark (0344). 

Vented Vial Adapter Indications, Safety and Warnings

Rx Only

Vial Adapters are 510(k) cleared by the United States Food and Drug Administration and carry the CE mark (0344). Products are shown for INFORMATION purposes only and may not be approved for marketing in specific regions. Distribution and use are subject to applicable regulatory approvals and requirements for medical devices. The Vial Adapter is configurable and may not be suitable for use with all drugs. Refer to drug manufacturer's labeling and use instructions for device configuration compatibility. Failure to follow product instructions for use may result in compromised sterility; contamination; leakage (including possible exposure to medication); and/or inadequate medication reconstitution, transfer, and/or dosing. Product misuse could potentially lead to user and/or patient infection, suboptimal therapy, and/or delay in therapy. Please contact your West Pharmaceutical Services, inc. (West) representative for product availability. Important product and safety information and warnings at: https://www.westpharma.com/products/vial-adapter-systems/vial-adapters.

• Consists of the vial adapter body with a single lumen piercing spike and a swabable valve which allows multiple needle-free accesses to drug vial to facilitate the addition or withdraw of medication for treatment.
• The device plastic package and cover are designed to maintain sterility and to assist in attaching the device to the drug vial.
• Vial adapters are 510(k) cleared by the United States Food and Drug Administration and carries the CE mark (0344). 

Swabable Vial Adapter Indication, Safety and Warnings

Rx Only

Vial Adapters are 510(k) cleared by the United States Food and Drug Administration and carry the CE mark (0344). Products are shown for INFORMATION purposes only and may not be approved for marketing in specific regions. Distribution and use are subject to applicable regulatory approvals and requirements for medical devices. The Swabable Vial Adapter inhibits microbial ingress for up to 24 hours when used in accordance with the product instructions for use and proper aseptic technique. The use of the Swabable Vial Adapter should not be interpreted as modifying, extending, or superseding a drug manufacturer's labeling recommendations for storage and expiration dating. The Swabable Vial Adapter is not compatible for use with all drug products. Refer to drug manufacturer's labeling and use instructions for shelf life and sterility information of opened or reconstituted drug product and for device compatibility. Failure to follow product instructions for use may result in compromised sterility, contamination, leakage (including possible exposure to medication), inadequate medication reconstitution, transfer, and/or dosing. Product misuse could potentially lead to user and/or patient infection, suboptimal therapy, and/or delay in therapy. Please contact your West Pharmaceutical Services, inc. (West) representative for product availability. Important product and safety information and warnings at: https://www.westpharma.com/products/vial-adapter-systems/vial-adapters.