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Standard Internal Hex Plastic Surgical Kit-Starter

by Medigma Biomedical GmbH EUDAMED

Active European Union

Ref SURPSModel Tools, Kit

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-DEMF000009412SURPSCX Basic UDI-DIDate21 Jun 2022RegisteredStatusActive
European UnionCE/MDD NumberB-DEMF000009412SURPSCX Basic UDI-DIDate21 Jun 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

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.

Specification

EUDAMED

Device Name
Tools
Model / Reference
Tools, SURPS, Kit
Primary DI / UDI-DI
D-DEMF000009412SURPSCX, 04260525162843
Basic UDI-DI
B-DEMF000009412SURPSCX, 426052516FullKitFK
EMDN Code
Z12110180, L159016
Device Class
Class IIa
Market of Registration
Türkiye
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000009412

Other devices from Medigma Biomedical GmbH

See all devices from Medigma Biomedical GmbH →

Properties

  • Reusable YesEUDAMEDNoEUDAMED

Other properties (12)

  • Sterile: No
  • Implantable: 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