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L100019A

by provita medical gmbh & co. kg

Ref 207241

L100019A (207241) is a Class I device made by provita medical gmbh & co. kg, registered in EUDAMED on 6 Jul 2026 (Basic UDI-DI 42601239314JD), 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 Number42601239314JD Basic UDI-DI 04260123930721UDI-DIDate6 Jul 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  • Withdrawn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

Device name
Lights mobile + accessories
Model / reference
207241
Primary DI / UDI-DI
04260123930721
Basic UDI-DI
42601239314JD
Direct marketing DI
04260123930721
EMDN code
Z12010702 Mobile scialytic lamps
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005332

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Properties

Other properties (14, all answered No)