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KEYU Iodine Solution

EUDAMED

Class A (EU MDR)

Ref KU-FI01

by Zhuhai Keyu Biological Engineering Co., Ltd

Identity

Trade Name
KEYU Iodine Solution EUDAMED
Device Name
Iodine Solution EUDAMED
Model / Reference
KU-FI01 EUDAMED

Identifiers

Primary DI / UDI-DI
06974735361474 EUDAMED
Basic UDI-DI
697473536KUC13PM EUDAMED
EMDN Code
W01019099 CLINICAL CHEMISTRY REAGENTS - OTHER 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

Category: Nucleic acid extraction/isolation kit IVD

KEYU Iodine Solution by Zhuhai Keyu Biological Engineering Co., Ltd — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid extraction/isolation kit IVD.

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 ed00e7b8-647b-489c-b595-e50f1ea161e0 61 fields · synced Jun 17, 2026