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iFlash-tTG IgG

EUDAMED

Class B (EU MDR)

Ref C86072GRef C86072G-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-tTG IgG EUDAMED
Device Name
iFlash-tTG IgG EUDAMED
Model / Reference
C86072G EUDAMED
C86072G-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912716723 EUDAMED
06925912721413 EUDAMED
Basic UDI-DI
692591270119HB EUDAMED
EMDN Code
W0102100601 TISSUE TRANSGLUTAMINASE 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

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

New Device

No

EUDAMED

iFlash-tTG IgG 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 dad7d3ea-1ac2-4aef-98c3-29e56c0b4617 61 fields · synced Aug 3, 2026
  • EUDAMED 59186766-9a19-47ec-98a2-0cc1d67de714 61 fields · synced Aug 3, 2026