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Culture Bottle

EUDAMED

Class A (EU MDR)

Ref TDR Resin Peds

by Hunan Mindray Medical Technology Co., Ltd.

Identity

Device Name
Culture Bottle EUDAMED
Model / Reference
TDR Resin Peds EUDAMED

Identifiers

Primary DI / UDI-DI
06938010901700 EUDAMED
Basic UDI-DI
69380109017004W EUDAMED
EMDN Code
W0104010504 BOTTLES FOR AUTOMATED BLOOD CULTURE EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Poland 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

Culture Bottle by Hunan Mindray Medical Technology Co., Ltd. — Class A — CE/MDR — 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

EUDAMED SRN
CN-MF-000022479
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 8bd26700-5707-4820-b02c-3d4f11e5dc46 61 fields · synced Oct 6, 2026