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iFlash-DGP IgA

EUDAMED

Class B (EU MDR)

Ref C86073ARef C86073A-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-DGP IgA EUDAMED
Device Name
iFlash-DGP IgA EUDAMED
Model / Reference
C86073A EUDAMED
C86073A-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912716761 EUDAMED
06925912721383 EUDAMED
Basic UDI-DI
692591270116H5 EUDAMED
EMDN Code
W0102100699 CELIAC DISEASE - OTHER 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-DGP IgA 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

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Manufacturer

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

Sources (2)

  • EUDAMED 2b47832d-5d81-44c7-977d-549fc5b8e666 61 fields · synced Jul 11, 2026
  • EUDAMED 75e5d06e-1a5e-4611-b885-525c57d3daaf 61 fields · synced Jul 9, 2026