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iFlash-PCNA IgG

EUDAMED

Class B (EU MDR)

Ref C86108Ref C86108-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-PCNA IgG EUDAMED
Device Name
iFlash-PCNA IgG EUDAMED
Model / Reference
C86108 EUDAMED
C86108-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912720232 EUDAMED
06925912721536 EUDAMED
Basic UDI-DI
692591270264HM EUDAMED
EMDN Code
W0102109099 AUTO-IMMUNE DISEASE TESTS - 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

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-PCNA 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 4248e447-78d5-4918-b698-4553b878a478 61 fields · synced Jul 20, 2026
  • EUDAMED a8c3cd6b-75bc-4afb-aa4e-2311d6dea60a 61 fields · synced May 18, 2026