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Prealbumin Reagent Kit

EUDAMED

Class IVD General (EU MDR)

Ref PA6011Y, PA6012Y, PA6013Y, PA6014Y, PA6015Y, PA6011N, PA6012N, PA6013N, PA6014N, PA6015N

by Hangzhou Aichek Medical Technology Co., Ltd.

Identity

Trade Name
Prealbumin Reagent Kit EUDAMED
Device Name
Prealbumin Reagent Kit EUDAMED
Model / Reference
PA6011Y, PA6012Y, PA6013Y, PA6014Y, PA6015Y, PA6011N, PA6012N, PA6013N, PA6014N, PA6015N EUDAMED

Identifiers

Primary DI / UDI-DI
D-PA601UK EUDAMED
Basic UDI-DI
B-PA601UK EUDAMED
EMDN Code
W0102010305 PRE-ALBUMIN / TRANSTHYRETIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Prealbumin Reagent Kit by Hangzhou Aichek Medical Technology 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-000028093
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (2)

  • EUDAMED e3d0fc3f-1a70-4622-8491-7286c8dffa6b 61 fields · synced Jun 17, 2026
  • EUDAMED e3d0fc3f-1a70-4622-8491-7286c8dffa6b-1 61 fields · synced Jun 9, 2026