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Foot Pedal

by G.N.S neoLaser Ltd.

Ref BG11050

Foot Pedal (BG11050) is a Class I device made by G.N.S Neolaser Ltd, registered in EUDAMED on 25 May 2026 (Basic UDI-DI 729001662940BS), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number729001662940BS Basic UDI-DI 07290016629408UDI-DIDate25 May 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
BG11050
Primary DI / UDI-DI
07290016629408
Basic UDI-DI
729001662940BS
Direct marketing DI
07290016629408
EMDN code
Z12011080 Laser surgery instruments - hardware accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000009852
Authorised representative
MedNet EC-REP IIb GmbH DE-AR-000011192

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Properties

Other properties (14, all answered No)