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DSA2000

by Dental International EUDAMED 2 variants

Active European Union

Ref DSA2000

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number87193275323DSA2000GR Basic UDI-DIDate9 Aug 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Model / Reference
DSA2000
Primary DI / UDI-DI
08720299542327, 08720299542396, 08720299542389, 08720299542372, 08720299542341, 08720299542365, 08720299542334
Basic UDI-DI
87193275323DSA2000GR
Direct Marketing DI
08720299542327
08720299542396
08720299542389
08720299542372
08720299542341
08720299542365
08720299542334
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class I
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000010964

Other devices from Dental International

See all devices from Dental International →

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