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Perfection Plus RestorePLUS

by Perfection Plus United Kingdom EUDAMED

Ref 010/1700

EMDN Q01010103

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060503730502 Basic UDI-DIDate7 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
Perfection Plus RestorePLUS Syringe
Model / Reference
010/1700
Primary DI / UDI-DI
05060503730502
Basic UDI-DI
B-05060503730502
EMDN Code
Q01010103 Dental restorative composites
Device Class
Class IIa
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000023781
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Perfection Plus

See all devices from Perfection Plus →

Properties & raw data

Show properties, registry sources and raw records
  • Implantable
Other properties (10)
  • Sterile: 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

Sources (1)

  • EUDAMED 05060503730502|B-05060503730502 61 fields · synced 25 Oct 2026