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IgE Rapid Test Device - serum

EUDAMED

Class IVD General (EU MDR)

Ref D020501D

by Hangzhou Cybereagen Biotech Co., Ltd.

Identity

Trade Name
IgE Rapid Test Device (whole blood/serum/plasma) EUDAMED
Model / Reference
D020501D EUDAMED

Identifiers

Primary DI / UDI-DI
06976753472927 EUDAMED
Basic UDI-DI
B-06976753472927 EUDAMED
EMDN Code
W0102010199 IMMUNOGLOBULINS - OTHER EUDAMED
Models / Variants
whole blood EUDAMED
serum EUDAMED
plasma EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

IgE Rapid Test Device - serum by Hangzhou Cybereagen Biotech Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — 3 models — 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-000037850
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED c5484a58-fc6a-42ef-b9e2-0eea7de4c0bb 61 fields · synced Jun 18, 2026