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iFlash-IGF-1

EUDAMED

Class B (EU MDR)

Ref C86135-SRef C86135

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-IGF-1 EUDAMED
Device Name
iFlash-IGF-1 EUDAMED
Model / Reference
C86135-S EUDAMED
C86135 EUDAMED

Identifiers

Primary DI / UDI-DI
06925912720607 EUDAMED
06925912720034 EUDAMED
Basic UDI-DI
692591270256HN EUDAMED
EMDN Code
W0102060403 INSULIN-LIKE GROWTH FACTOR I (SOMATOMEDIN C) 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

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-IGF-1 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 6fd9f648-ca14-40c1-ae80-f2b9778d2251 61 fields · synced Jul 9, 2026
  • EUDAMED 210c812b-0808-44ac-b775-737ae34bb0f4 61 fields · synced May 17, 2026