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Anaerogen 3.5l 10 Pack

EUDAMEDFDA UDI

Class A (EU MDR)

Ref AN0035A

by Oxoid Ltd

Identity

Trade Name
ANAEROGEN 3.5L 10 PACK EUDAMEDFDA UDI
Generic Name
Atmospheric generation kit IVD FDA UDI
Device Name
ANAEROGEN EUDAMED
Model / Reference
AN0035A EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05032384028672 EUDAMEDFDA UDI
Basic UDI-DI
5032384AnaerogenCompactSV EUDAMED
FDA Product Code
KZJ FDA UDI
EMDN Code
W0104010999 ENVIRONMENTAL GENERATING SYSTEMS - OTHER EUDAMED
GMDN Term
Atmospheric generation kit IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
866.2580 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

No

EUDAMED

Reagent

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Anaerogen 3.5l 10 Pack by Oxoid Ltd — Class A — 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 e55abbb2-0aa7-4e62-828b-747fa8f80ab8 61 fields · synced Jun 19, 2026
  • FDA UDI 37fd1c18-db5d-4f56-b1a9-d7c2dd68a9bf 32 fields · synced May 30, 2026