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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
Medication transfer needle, filtering/vented FDA UDI
Device Name
VA 20mm Vented FLL w/o filter- SF FDA UDI
Model / Reference
8073017 FDA UDI
Description
VA 20mm Vented FLL w/o filter- SF FDA UDI

Identifiers

Primary DI / UDI-DI
07290108240368 FDA UDI
510(k) Number
K062482 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Medication transfer needle, filtering/vented FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
Not 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
Sterilization Method
Radiation Sterilization FDA UDI

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

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 53f7cdea-84df-48a2-820b-b717ca119c4c 35 fields · synced May 30, 2026