Swabable Vented Vial Adapter

GUDID 27290108240102

Vial Adapter 20mm Vented Swabable – VF

WEST PHARMA. SERVICES IL, . LTD

Vial transfer spike Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented Medication transfer needle, filtering/vented

• Primary Device ID: 27290108240102
• NIH Device Record Key: 00cb5e22-5ada-4920-a5af-c58cc1ea9464
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Swabable Vented Vial Adapter
• Version Model Number: 8073009
• Company DUNS: 600267793
• Company Name: WEST PHARMA. SERVICES IL, . LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290108240108 [Primary]
GS1	17290108240105 [Package]; Contains: 07290108240108; Package: [145 Units]; In Commercial Distribution
GS1	27290108240102 [Package]; Contains: 17290108240105; Package: [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072511

FDA Product Code

• LHI: Set, I.V. Fluid Transfer

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

[27290108240102]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-03-18
• Device Publish Date: 2016-05-01

On-Brand Devices [Swabable Vented Vial Adapter]

• 27290108240980: Swabable Vial Adapter 13mm with Vented Spike – VF
• 27290108240911: Swabable Vial Adapter 13mm with Vented Spike – VF
• 27290108240744: Swabable Vial Adapter 20mm with Vented Spike –VF
• 27290108240102: Vial Adapter 20mm Vented Swabable – VF