Vial2Bag Advanced 20mm

GUDID 20850022888018

Vial2Bag Advanced 20mm - Admixture Device

West Pharmaceutical Services Az, Inc.

Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic Vial/bottle adaptor, non-hermetic

• Primary Device ID: 20850022888018
• NIH Device Record Key: f654a494-5cfd-4548-b013-c5dd74b880e0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vial2Bag Advanced 20mm
• Version Model Number: 6070030
• Company DUNS: 063293484
• Company Name: West Pharmaceutical Services Az, Inc.
• 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	10850022888011 [Primary]
GS1	20850022888018 [Package]; Contains: 10850022888011; Package: Intermediate Box [50 Units]; In Commercial Distribution
GS1	30850022888015 [Package]; Package: Shipping Box [150 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201415

FDA Product Code

• LHI: Set, I.V. Fluid Transfer

Sterilization

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

[20850022888018]

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[20850022888018]

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[20850022888018]

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[20850022888018]

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[20850022888018]

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[20850022888018]

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[20850022888018]

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[20850022888018]

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[20850022888018]

Ethylene Oxide

[20850022888018]

Ethylene Oxide

[20850022888018]

Ethylene Oxide

[20850022888018]

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[20850022888018]

Ethylene Oxide

[20850022888018]

Ethylene Oxide

[20850022888018]

Ethylene Oxide

[20850022888018]

Ethylene Oxide

[20850022888018]

Ethylene Oxide

[20850022888018]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-12-31
• Device Publish Date: 2020-12-23