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iFlash-HSV-2 IgM

EUDAMED

Class C (EU MDR)

Ref C88039MRef C88039M-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-HSV-2 IgM EUDAMED
Device Name
iFlash-HSV-2 IgM EUDAMED
Model / Reference
C88039M EUDAMED
C88039M-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912718994 EUDAMED
06925912723547 EUDAMED
Basic UDI-DI
692591270060H3 EUDAMED
EMDN Code
W0105040310 HSV 2 IGM 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-HSV-2 IgM 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 0d82e183-67e0-4c52-bf55-625771bc0c38 61 fields · synced Jul 8, 2026
  • EUDAMED 5b4ba2fe-0325-4f6c-8bb1-73b7696d54b4 61 fields · synced Jun 18, 2026