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PLDD Set

by Radimed Gesellschaft für Kommunikationsdienstleistungen und Medizintechnik mbH 3 variants

Ref 10105-22

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426014668SETPLDDNT Basic UDI-DI 04260146685318UDI-DIDate17 Sep 2026RegisteredStatusActive

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

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
PLDD Set
Model / Reference
10105-22
Primary DI / UDI-DI
04260146685318
Basic UDI-DI
426014668SETPLDDNT
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIa
Medical Purpose
Set for Percutaneous Laser Disc Decompression

Manufacturer details

EUDAMED SRN
DE-PR-000058930

From the manufacturer

Manufacturer's product page: Sets & Laserfasern PLDD

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Properties

Other properties (1)

  • Sterile: No