Skip to content

Bonasil A+ Light HTS (FS) 50ml x 2

by DMP Dental Industry S.A. EUDAMED

Active European Union

Ref 210112010F

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5206569DSIL22SD Basic UDI-DIDate21 May 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  • Withdrawn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

Device Name
Addition Curing Silicone Impression Material
Model / Reference
210112010F
Primary DI / UDI-DI
05206569450019
Basic UDI-DI
5206569DSIL22SD
EMDN Code
Q01020102 Dental impression vinylsiloxans
Device Class
Class I
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000019283

Other devices from Dmp Dental Industry S.A.

See all devices from Dmp Dental Industry S.A. →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No