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Vented Vial Adapter Transfer Device

FDA UDI

Class II (US FDA UDI)

by West Pharma. Services Il, . Ltd

Identity

Trade Name
Vented Vial Adapter Transfer Device FDA UDI
Generic Name
Vial/bottle adaptor, hermetic FDA UDI
Device Name
Vented Vial Adapter 20mm FLL- VF FDA UDI
Model / Reference
8073051 FDA UDI
Description
Vented Vial Adapter 20mm FLL- VF FDA UDI

Identifiers

Catalog Number
8073051 FDA UDI
Primary DI / UDI-DI
07290108241334 FDA UDI
510(k) Number
K062482 FDA UDI
K213513 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Vial/bottle adaptor, hermetic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vial/bottle adaptor, hermetic

Vented Vial Adapter Transfer Device by West Pharma. Services Il, . Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vial/bottle adaptor, hermetic.

Cleared under the same submission

K062482 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
West Pharma. Services Il, . Ltd

Sources (1)

  • FDA UDI 48d94271-59ac-4548-9cdb-bb996a4b0368 36 fields · synced May 30, 2026