Katakit 1

by GFAP France

Ref PRK-KK1

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number3770043317PRK-KK1CS Basic UDI-DI 03770043317003UDI-DI	Date24 Aug 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: PRK-KK1

Primary DI / UDI-DI: 03770043317003
Basic UDI-DI: 3770043317PRK-KK1CS
EMDN Code: V0501 Clinical emergency kits

Device Class: Class IIa
Medical Purpose: Disaster preparedness and first aid kit

Manufacturer details

EUDAMED SRN: FR-PR-000052641

Other devices from GFAP France

Katakit 4

Class IIa
Frc-CK1

Class I
Frc-CK4

Class I

Properties

Other properties (1)

Sterile: No