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Perfectha Lidocaine

by Sinclair France SAS France EUDAMED

Ref PDLModel Derm Lidocaine EMDN X0303

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50600330436271809612140N4 Basic UDI-DIDate23 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Perfectha Derm Lidocaine
Model / Reference
Derm Lidocaine, PDL
Primary DI / UDI-DI
05060033044797
Basic UDI-DI
50600330436271809612140N4
EMDN Code
X0303 Substances, combinations of substances, or items without an intended medical purpose intended to be used for facial or other dermal or mucous membrane filling by subcutaneous, submucous or intradermal injection or other introduction, by a prefilled means for introduction, excluding those for tattooing – resorbable
Device Class
Class III
Medical Purpose
Perfectha Lidocaine product range is intended for facial filling by subcutaneous, submucous, intradermal or supraperiosteal injection. Perfectha Lidocaine is implanted in the areas of the face to fill skin depressions, wrinkles, and fine lines, and for the augmentation of tissue volume.

Manufacturer details

EUDAMED SRN
FR-PR-000053000

Other devices from Sinclair France SAS

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Properties & raw data

Show properties, registry sources and raw records
  • Sterile

Sources (1)

  • EUDAMED c779866f-a46c-4550-aed9-08663efad5f3 61 fields · synced 22 Oct 2026