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Sterile gauze swabs

EUDAMED

Class I (EU MDR)

Ref 17C02:10cm×10cm-8P

by Fomed Industries Inc.

Identity

Device Name
Sterile gauze swabs EUDAMED
Model / Reference
17C02:10cm×10cm-8P EUDAMED

Identifiers

Primary DI / UDI-DI
06973685040675 EUDAMED
Basic UDI-DI
697368504SBPWXCS01FH EUDAMED
Unit of Use DI
06973685040705 EUDAMED
EMDN Code
M0201020101 COTTON GAUZES, FOLDED, WITHOUT X-RAY DETECTABLE THREAD, STERILE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Sterile gauze swabs by Fomed Industries Inc — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000012944
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED a1ded03e-b0c9-4043-93c8-bb0c81495cae 61 fields · synced Jun 19, 2026