← Back to catalogue

Swabable Vented Vial Adapter™

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 8073009

by West Pharma. Services IL, Ltd.

Identity

Trade Name
Swabable Vented Vial Adapter™ EUDAMED
Swabable Vented Vial Adapter FDA UDI
Generic Name
Medication transfer needle, filtering/vented FDA UDI
Device Name
Swabable Vented Vial Adapter™ EUDAMED
Vial Adapter 20mm Vented Swabable – VF FDA UDI
Model / Reference
8073009 EUDAMEDFDA UDI
Description
Vial Adapter 20mm Vented Swabable – VF FDA UDI

Identifiers

Primary DI / UDI-DI
07290108241693 EUDAMED
07290108240108 FDA UDI
Basic UDI-DI
729010824SVVA20VF2D EUDAMED
510(k) Number
K072511 FDA UDI
FDA Product Code
LHI FDA UDI
EMDN Code
A0704 SYSTEMS FOR RECONSTITUTION AND ADMINISTRATION OF PHARMACEUTICALS EUDAMED
GMDN Term
Medication transfer needle, filtering/vented FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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
Ethylene Oxide FDA UDI

Swabable Vented Vial Adapter™ by West Pharma. Services IL, Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IL-MF-000008572
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED abf8b469-b5b6-467e-9f05-b764d4e2b8c1 61 fields · synced Jul 9, 2026
  • FDA UDI 00cb5e22-5ada-4920-a5af-c58cc1ea9464 35 fields · synced May 30, 2026