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Sampling Cup

EUDAMED

Class A (EU MDR)

Ref M02001-02

by Shenzhen Reetoo Biotechnology Co., Ltd

Identity

Device Name
Sampling Cup EUDAMED
Model / Reference
M02001-02 EUDAMED

Identifiers

Primary DI / UDI-DI
06974675460343 EUDAMED
Basic UDI-DI
697467546S80201GL EUDAMED
EMDN Code
W05010299 URINE COLLECTION DEVICES - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

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

Sampling Cup by Shenzhen Reetoo Biotechnology Co., 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

EUDAMED SRN
CN-MF-000011699
Authorised Representative
Umedwings Netherlands B.V. NL-AR-000000444

Sources (1)

  • EUDAMED 2c17616e-d7e8-4065-9d31-e64f551f9994 61 fields · synced Jun 19, 2026