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KEYU Sample Collection Tube

EUDAMED

Class A (EU MDR)

Ref KU-F03-I

by Zhuhai Keyu Biological Engineering Co., Ltd

Identity

Trade Name
KEYU Sample Collection Tube EUDAMED
Device Name
Sample Collection Tube EUDAMED
Model / Reference
KU-F03-I EUDAMED

Identifiers

Primary DI / UDI-DI
06974735361498 EUDAMED
Basic UDI-DI
697473536KUC15PR EUDAMED
EMDN Code
W05019001 FAECES COLLECTION DEVICES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain 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

KEYU Sample Collection Tube by Zhuhai Keyu Biological Engineering 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-000023195
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 2c18a076-3dd9-4798-b4a8-67fb655e5760 61 fields · synced Jun 19, 2026