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Impression Coping Analog

by Ditron Dental Ltd. 5 variants

Ref SRA-ANA480Model Impression Coping Analog

Active European Union

CE MDR

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/MDR Number729010928ANAHF Basic UDI-DIDate14 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Implant Analog Internal Hex.
Model / Reference
Impression Coping Analog, SRA-ANA480
Primary DI / UDI-DI
07290122086935
Basic UDI-DI
729010928ANAHF
Direct Marketing DI
07290122086935
EMDN Code
Q010599 Dental instruments, single-use - other
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000015966
Authorised representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Other devices from Ditron Dental Ltd

See all devices from Ditron Dental Ltd →

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