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GFAP France

Francefrom SRN

Devices
4

What GFAP France makes

GFAP France manufactures reusable surgical drapes and gowns designed for single-use applications in medical settings, including the FRC-CK1 and FRC-CK4 models. These products are intended to provide barrier protection during surgical procedures and other clinical interventions.

The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class I devices and is registered in the EU’s eudamed database. The products are developed and distributed from France.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • Katakit 4 Ref PRK-KK4

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Katakit 1 Ref PRK-KK1

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Frc-CK1

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Frc-CK4

    Active Regimes: CE MDR Registry: EUDAMED Class:I

Frequently asked questions

How many devices does GFAP France have in the registry?

The registry currently lists 4 devices for GFAP France. Devices recorded under merged duplicate company entries are counted once.

Which registries list GFAP France's devices?

Among its 4 most recently registered devices, GFAP France has devices listed in EUDAMED (4 devices).

What risk classes do GFAP France's devices fall under?

Among its 4 most recently registered devices, the classes recorded for GFAP France's devices are Class I and Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from GFAP France in the registry?

The most recently registered devices listed for GFAP France include Katakit 4, Katakit 1, FRC-CK1 and FRC-CK4.

Generated automatically from registry data and not verified by a human reviewer.