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SafeFix

EUDAMED

Class A (EU MDR)

Ref CSFA

by Noul Co., Ltd.

Identity

Trade Name
SafeFix EUDAMED
Device Name
SafeFix EUDAMED
Model / Reference
CSFA EUDAMED

Identifiers

Primary DI / UDI-DI
08800100120019 EUDAMED
Basic UDI-DI
88001001AC001Z5 EUDAMED
EMDN Code
W01030705 FIXING REAGENTS (HISTOLOGY/CYTOLOGY) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

SafeFix by Noul Co., Ltd. — Class A — 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

Manufacturer
Noul Co., Ltd.
EUDAMED SRN
KR-MF-000033621
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED e779821a-1cfa-4c60-be8f-e2d152ca23a7 61 fields · synced Jul 10, 2026