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iFlash-Tg

EUDAMED

Class B (EU MDR)

Ref C86027-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-Tg EUDAMED
Device Name
iFlash-Tg EUDAMED
Model / Reference
C86027-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912723516 EUDAMED
Basic UDI-DI
692591270006GV EUDAMED
EMDN Code
W01020408 THYROGLOBULIN EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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-Tg 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 (1)

  • EUDAMED 040226fd-c6f0-4d20-a7e2-6c26ad416082 61 fields · synced Aug 2, 2026