← Back to catalogue

iFlash-IA-2A

EUDAMED

Class B (EU MDR)

Ref C89049GRef C89049G-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-IA-2A EUDAMED
Device Name
iFlash-IA-2A EUDAMED
Model / Reference
C89049G EUDAMED
C89049G-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912718963 EUDAMED
06925912723523 EUDAMED
Basic UDI-DI
692591270053H6 EUDAMED
EMDN Code
W0102060106 THYROSIN PHOSPHATASE IA2 ANTIBODIES EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

New Device

No

EUDAMED

iFlash-IA-2A by Shenzhen Yhlo Biotech Co., Ltd. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000001137
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED facf2cf6-2740-42d2-b55a-ebb6b1041b6a 61 fields · synced Jul 21, 2026
  • EUDAMED 2af91bef-f91c-46fc-8b6a-1e80e595cbbd 61 fields · synced Jul 20, 2026