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iFlash-Total PSA

EUDAMED

Class C (EU MDR)

Ref C86000Ref C86000-L

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-Total PSA EUDAMED
Device Name
iFlash-Total PSA EUDAMED
Model / Reference
C86000 EUDAMED
C86000-L EUDAMED

Identifiers

Primary DI / UDI-DI
06925912719250 EUDAMED
06925912715917 EUDAMED
Basic UDI-DI
692591270097HS EUDAMED
EMDN Code
W0102030113 TOTAL PROSTATIC SPECIFIC ANTIGEN 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

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-Total PSA 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

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Manufacturer

EUDAMED SRN
CN-MF-000001137
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED c9ca31b2-cfc8-47d2-9a14-c85db99b23cc 61 fields · synced Jul 22, 2026
  • EUDAMED 6434e592-860b-48e2-8f7d-6a2651f92139 61 fields · synced Jul 22, 2026