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Palga Protocol Plaveiselcelcarcinoom van de huid

by Stichting Palga

Ref Palga Protocol Plaveiselcelcarcinoom van de huid

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, self-declared

Class I: no certifier involved

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/MDD NumberB-08721325993274 Basic UDI-DI 08721325993274UDI-DIDate2 Oct 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Palga Protocol Plaveiselcelcarcinoom van de huid
Model / Reference
Palga Protocol Plaveiselcelcarcinoom van de huid
Primary DI / UDI-DI
08721325993274
Basic UDI-DI
B-08721325993274
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class I
Special Device Type
-1192
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000053903

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Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No