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Purified Water

EUDAMED

Class A (EU MDR)

Ref BO0209MRef BO1336ERef BO0209V

by Oxoid Ltd

Identity

Trade Name
PURIFIED WATER EUDAMED
Device Name
PURIFIED WATER EUDAMED
Model / Reference
BO0209M EUDAMED
BO1336E EUDAMED
BO0209V EUDAMED

Identifiers

Primary DI / UDI-DI
05032384018406 EUDAMED
05032384511860 EUDAMED
05032384056736 EUDAMED
Basic UDI-DI
5032384PurifiedWaterXR 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

No

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

Purified 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 (3)

  • EUDAMED e6c8932a-96fc-424f-aad3-c0dd553ec876 61 fields · synced Jul 12, 2026
  • EUDAMED 6416112b-c19f-498d-b67d-ca41e9a03362 61 fields · synced May 17, 2026
  • EUDAMED b9b96386-f30d-439d-bb6a-de6a407a01bc 61 fields · synced May 17, 2026