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Ø3.2 DYNA HELIX DC ART OCTA IMPLANT 10mm

by Dyna Dental Engineering B.V.

Ref 43210DCModel Dental Implants

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-EDYN43210DC0 Basic UDI-DI EDYN43210DC0UDI-DIDate22 Jul 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Ø3.2 DYNA HELIX DC ART OCTA IMPLANT 10mm
Model / Reference
Dental Implants, 43210DC
Primary DI / UDI-DI
EDYN43210DC0
Basic UDI-DI
B-EDYN43210DC0
EMDN Code
P01020101 Dental implants
Device Class
Class IIb
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000000527

From the manufacturer

Manufacturer's product page: Dyna Helix DC

Other devices from Dyna Dental Engineering B.V.

See all devices from Dyna Dental Engineering B.V. →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • 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