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iFlash-Chlamydia pn. IgM

EUDAMED

Class C (EU MDR)

Ref C88014MRef C88014M-L

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-Chlamydia pn. IgM EUDAMED
Device Name
iFlash-Chlamydia pn. IgM EUDAMED
Model / Reference
C88014M EUDAMED
C88014M-L EUDAMED

Identifiers

Primary DI / UDI-DI
06925912719229 EUDAMED
06925912715788 EUDAMED
Basic UDI-DI
692591270100GN EUDAMED
EMDN Code
W0105010116 CHLAMYDIA PNEUMONIAE ANTIBODY 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

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-Chlamydia pn. 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 6023c3d4-b8e0-42d5-9fb2-543ecad6ba72 61 fields · synced Jul 15, 2026
  • EUDAMED d20f8011-2c90-434d-bab4-7c811efeb717 61 fields · synced Jul 15, 2026