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Maximum Recovery Diluent

EUDAMED

Class A (EU MDR)

Ref BO0348ZRef CM0733TRef CM0733R

by Oxoid Ltd

Identity

Trade Name
MAXIMUM RECOVERY DILUENT EUDAMED
Device Name
MAXIMUM RECOVERY DILUENT EUDAMED
Model / Reference
BO0348Z EUDAMED
CM0733T EUDAMED
CM0733R EUDAMED

Identifiers

Primary DI / UDI-DI
05032384019304 EUDAMED
05032384058037 EUDAMED
05032384003983 EUDAMED
Basic UDI-DI
5032384MaxRecDilOL28 EUDAMED
EMDN Code
W0104010306 CULTURE MEDIA IN BOTTLES EUDAMED
W0104010101 DEHYDRATED CULTURE MEDIA (DCM) 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

Maximum Recovery Diluent 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 9344e7a4-d797-4269-b0bd-6b483fb9237b 61 fields · synced Jul 16, 2026
  • EUDAMED 670f91b9-2c5c-43d5-8e5d-eb44550b00f9 61 fields · synced May 17, 2026
  • EUDAMED cc20f40c-d3bd-410b-a983-74a4743f7e9b 61 fields · synced Jul 14, 2026