西林瓶适配器
West's 20mm and 13 mm vial adapters

西林瓶适配器

用于从西林瓶快速安全转移的解决方案

A close up image of lyophilized stoppers
概述
Vial Adapter™ and Ready Pack® are trademarks or registered trademarks of West Pharmaceutical Services Inc., in the United States and other jurisdictions
Vial Adapter Indication, Safety and Warnings
Vented Vial Adapter Indications, Safety and Warnings
Swabable Vial Adapter Indications, Safety and Warnings
Daikyo Crystal Zenith® is a registered trademark of Daikyo Seiko, Ltd.
West Ready Pack™ is a trademark of West Pharmaceutical Services, Inc., in the United States and other jurisdictions.
Mix2Vial® and Mixject® are registered trademarks of West Pharma. Services IL, Ltd., a subsidiary of West Pharmaceutical Services, Inc.


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.
Vented 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 Vented 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.
Swabable 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.

Technical Information

Container Closure Integrity Testing

Sterilization

Gamma irradiation is used for all configurations except Swabbable, which is sterilized using Ethylene Oxide (EtO).

Container Closure Integrity Testing

Materials of Construction

Vial Adapters are primarily constructed from medical‑grade polycarbonate. Depending on configuration, additional materials may be incorporated into the device assembly. A detailed materials list is available upon request.

Container Closure Integrity Testing

Shelf‑Life

Typical shelf‑life is 5 years based on validated packaging and stability testing. Check with our experts to confirm based on your configuration needs.

Technical Information

Container Closure Integrity Testing

Sterilization

Gamma irradiation is used for all configurations except Swabbable, which is sterilized using Ethylene Oxide (EtO).

Container Closure Integrity Testing

Materials of Construction

Vial Adapters are primarily constructed from medical‑grade polycarbonate. Depending on configuration, additional materials may be incorporated into the device assembly. A detailed materials list is available upon request.

Container Closure Integrity Testing

Shelf‑Life

Typical shelf‑life is 5 years based on validated packaging and stability testing. Check with our experts to confirm based on your configuration needs.