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Screw Driver for Machine

by SEWONMEDIX Inc. 30 variants

Ref MHD125MModel IH IMPLANT SYSTEM

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800041362295 Basic UDI-DI 08800041362295UDI-DIDate25 Apr 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
IH IMPLANT SYSTEM, MHD125M
Primary DI / UDI-DI
08800041362295
Basic UDI-DI
B-08800041362295
EMDN Code
L159016 Dental surgery instrument kits, reusable
Device Class
Class IIa
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
KR-MF-000016194
Authorised representative
Advena Limited MT-AR-000000234

Related devices

Category: Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Other devices from SEWONMEDIX Inc.

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Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No