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Immunoglobulin A (IgA) Assay kit (Immunoturbidimetric Method)

EUDAMED

Class IVD General (EU MDR)

Ref R1: 2×60 mL, R2: 2×20 mL

by Shenzhen AmTech Bioengineering Ltd., Inc.

Identity

Device Name
Immunoglobulin A (IgA) Assay kit (Immunoturbidimetric Method) EUDAMED
Model / Reference
R1: 2×60 mL, R2: 2×20 mL EUDAMED

Identifiers

Primary DI / UDI-DI
06937287300117 EUDAMED
Basic UDI-DI
B-06937287300117 EUDAMED
EMDN Code
W0102010101 IMMUNOGLOBULIN A 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

Immunoglobulin A (IgA) Assay kit (Immunoturbidimetric 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 5bee38b0-d52b-471c-b8a0-b99e86376f9e 61 fields · synced Jun 18, 2026
  • EUDAMED 5bee38b0-d52b-471c-b8a0-b99e86376f9e-1 61 fields · synced Jun 10, 2026