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Tissue Implant Ø5, 3/L13 Wp

by Mode Medi̇kal San. Ve Ti̇c. Ltd. Şti̇

Ref 01.04.13.53Model RAPID IMPLANT Ø3,7/L10 NP

Expiring European Union

CE MDR

Valid until

8 May 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier UDEM Adriatic d.o.o.

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 NumberM.2023.MDR.1015 Date15 May 2026IssuedStatusExpiring expires 8 May 2027

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • M.2023.MDR.1015 Expiring Supplemented Expires in 188 days

    Quality management system EU MDR

    Certifier
    UDEM Adriatic d.o.o. 2696
    Issued
    15 May 2026
    Expires
    8 May 2027
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Expiring

Specification

EUDAMED

Device Name
Sterile Substructures- Implants
Model / Reference
RAPID IMPLANT Ø3, 7/L10 NP, 01.04.13.53
Primary DI / UDI-DI
08680617141222
Basic UDI-DI
868061714MODEIMPLANTF6
Direct Marketing DI
08680617141222
EMDN Code
P01020101 Dental implants
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000018719

Other devices from Mode Medi̇kal San. Ve Ti̇c. Ltd. Şti̇

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Properties

  • Sterile
  • Implantable
  • Sutures

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