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Alkaline Peptone Water

EUDAMED

Class A (EU MDR)

Ref BO0335E

by Oxoid Ltd

Identity

Trade Name
ALKALINE PEPTONE WATER EUDAMED
Device Name
ALKALINE PEPTONE WATER EUDAMED
Model / Reference
BO0335E EUDAMED

Identifiers

Primary DI / UDI-DI
05032384018987 EUDAMED
Basic UDI-DI
5032384AlkPeptoneWtrPPMSZ EUDAMED
EMDN Code
W0104010306 CULTURE MEDIA IN BOTTLES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

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

Alkaline Peptone Water by Oxoid Ltd — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

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

Sources (1)

  • EUDAMED ecf94925-2107-43ec-9653-6818e42d646b 61 fields · synced Aug 5, 2026