← Back to catalogue

iFlash-PIVKA-Ⅱ

EUDAMED

Class C (EU MDR)

Ref C86137-SRef C86137

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-PIVKA-Ⅱ EUDAMED
Device Name
iFlash-PIVKA-Ⅱ EUDAMED
Model / Reference
C86137-S EUDAMED
C86137 EUDAMED

Identifiers

Primary DI / UDI-DI
06925912721451 EUDAMED
06925912716884 EUDAMED
Basic UDI-DI
692591270184HN EUDAMED
EMDN Code
W0102030199 CANCER ANTIGENS - OTHER EUDAMED

Classification

Device Class
Class C 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-PIVKA-Ⅱ by Shenzhen Yhlo Biotech Co., Ltd. — Class C — 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 a6076259-f415-4b5d-a0c1-3df65bba05ea 61 fields · synced Jul 30, 2026
  • EUDAMED 8be882d9-1e53-4f5e-8f8a-777a07e94e88 61 fields · synced May 18, 2026