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Clinical Emergency Lyophilized Kit 15

EUDAMED

Class IVD General (EU MDR)

Ref EC-001

by Zhejiang Orient Gene Biotech Co., Ltd

Identity

Trade Name
Clinical Emergency Lyophilized Kit 15 EUDAMED
Device Name
Clinical Emergency Lyophilized Kit 15 EUDAMED
Model / Reference
EC-001 EUDAMED

Identifiers

Primary DI / UDI-DI
06950996050296 EUDAMED
Basic UDI-DI
B-06950996050296 EUDAMED
EMDN Code
W01010404 MULTIPLE PARAMETERS (MIX OF ALL) - CLIN. CHEM LAB R. EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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

Clinical Emergency Lyophilized Kit 15 by Zhejiang Orient Gene Biotech Co., Ltd — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000017965
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 7bff5dce-6241-47b3-915e-bef1b5075152 61 fields · synced Jun 18, 2026