← Back to catalogue

iFlash-Total β HCG

EUDAMED

Class C (EU MDR)

Ref C86327-L

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-Total β HCG EUDAMED
Device Name
iFlash-Total β HCG EUDAMED
Model / Reference
C86327-L EUDAMED

Identifiers

Primary DI / UDI-DI
06925912734338 EUDAMED
Basic UDI-DI
692591270279J2 EUDAMED
EMDN Code
W0102039099 TUMOUR MARKERS - OTHER EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

Category: Preferentially expressed antigen in melanoma (PRAME) IVD, antibody

iFlash-Total β HCG by Shenzhen Yhlo Biotech Co., Ltd. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Preferentially expressed antigen in melanoma (PRAME) IVD, antibody.

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 (1)

  • EUDAMED 12a37742-e36c-4d0b-971d-a72f653fdc15 61 fields · synced Jun 18, 2026