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V Factor

EUDAMEDFDA UDI

Class B (EU MDR)

Ref DD0004B

by Oxoid Ltd

Identity

Trade Name
V FACTOR EUDAMEDFDA UDI
Generic Name
V factor differentiation disc IVD FDA UDI
Device Name
V FACTOR EUDAMED
Model / Reference
DD0004B EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05032384104659 EUDAMEDFDA UDI
Basic UDI-DI
5032384VFactorDDRP EUDAMED
510(k) Number
K802501 FDA UDI
FDA Product Code
JTO FDA UDI
EMDN Code
W0104080208 SINGLE TESTS (DISCS, STRIPS, DROPPERS...) EUDAMED
GMDN Term
V factor differentiation disc IVD FDA UDI

Classification

Device Class
Class B EUDAMED
Class I FDA UDI
Regulation Number
866.2660 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Prescription Use

No

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

V Factor by Oxoid Ltd — Class B — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oxoid Ltd
EUDAMED SRN
GB-MF-000016914
Authorised Representative
Thermo Fisher Diagnostics B.V. NL-AR-000013157

Sources (2)

  • EUDAMED abe69466-4094-4dc8-9b5f-123c8b4155ad 61 fields · synced Jul 13, 2026
  • FDA UDI 2cbd137a-53c6-4ee3-9048-956ef9f2f7ea 33 fields · synced May 30, 2026