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Glutathione Reductase (GR) Assay Kit (Glutathione Substrate Method)

EUDAMED

Class IVD General (EU MDR)

Ref R1: 2×50 mL, R2: 2×10 mL

by Shenzhen AmTech Bioengineering Ltd., Inc.

Identity

Device Name
Glutathione Reductase (GR) Assay Kit (Glutathione Substrate Method) EUDAMED
Model / Reference
R1: 2×50 mL, R2: 2×10 mL EUDAMED

Identifiers

Primary DI / UDI-DI
06937287300087 EUDAMED
Basic UDI-DI
B-06937287300087 EUDAMED
EMDN Code
W01010199 ENZYMES - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria 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

Glutathione Reductase (GR) Assay Kit (Glutathione Substrate Method) by Shenzhen AmTech Bioengineering Ltd., Inc. — 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-000043067
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED 5258a1e3-6713-46ab-b7fe-3a8cab052e0d 61 fields · synced Jun 19, 2026
  • EUDAMED 5258a1e3-6713-46ab-b7fe-3a8cab052e0d-1 61 fields · synced Jun 10, 2026