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Angiotensin-converting Enzyme Test Kit (Rate Assay)

EUDAMED

Class IVD General (EU MDR)

Ref /

by Shanghai Kehua Bio-engineering Co., Ltd.

Identity

Device Name
Angiotensin-converting Enzyme Test Kit (Rate Assay) EUDAMED
Model / Reference
/ EUDAMED

Identifiers

Primary DI / UDI-DI
D-1767A EUDAMED
Basic UDI-DI
B-1767A EUDAMED
EMDN Code
W01010109 ANGIOTENSIN CONVERTING ENZYME (CC) EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Belgium 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

Angiotensin-converting Enzyme Test Kit (Rate Assay) by Shanghai Kehua Bio-engineering Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000026756
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 623f73ff-842b-46f7-bac7-aaa9256b2b1e 61 fields · synced Jul 29, 2026