Bi̇med

Ref 9054281-KK4

Active European Union

CE MDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-08699495021250 Basic UDI-DI	Date12 May 2026Registered	StatusActive

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.

1 jurisdiction

European Union — CE/MDD Active

EUDAMED

Device Name: 1000 dermatoloji prob ucu
1910 jinekoloji prob ucu
0612 dermatoloji probu
1200 dermatoloji prob ucu
oftalmoloji cryo probu (extended retina) 2,5mm
oftalmoloji cryo probu (mid-reach retina) 2,5mm
oftalmoloji cryo probu (straight cataract) 1,6mm
oftalmoloji cryo probu (glaucoma) 3,0mm
jinekoloji probu
oftalmoloji cryo probu (standart retina) 2,5mm
dermatoloji probu
oftalmoloji cryo probu (curved cataract) 1,6mm
0519 jinekoloji prob ucu
Model / Reference: 9054281-KK4

Primary DI / UDI-DI: 08699495021250, 08699495021168, 08699495021236, 08699495021267, 08699495021328, 08699495021335, 08699495021281, 08699495021342, 08699495021137, 08699495021311, 08699495021199, 08699495021298, 08699495021182
Basic UDI-DI: B-08699495021250, B-08699495021168, B-08699495021236, B-08699495021267, B-08699495021328, B-08699495021335, B-08699495021281, B-08699495021342, B-08699495021137, B-08699495021311, B-08699495021199, B-08699495021298, B-08699495021182
EMDN Code: Z120102 Cryosurgery equipment