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Mutars®

by implantcast GmbH Germany EUDAMED

Ref 76301000Model MUT07FCBINST

EMDN L0922

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4048844MUT07FCBINSTBU Basic UDI-DIDate20 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
-
Model / Reference
MUT07FCBINST, 76301000
Primary DI / UDI-DI
04048844060589
Basic UDI-DI
4048844MUT07FCBINSTBU
EMDN Code
L0922 Orthopaedic surgery guides, reusable
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
DE-MF-000010002

Other devices from implantcast GmbH

See all devices from implantcast GmbH →

Properties & raw data

Show properties, registry sources and raw records
  • Reusable
  • CMR Substance
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 04048844060589|4048844MUT07FCBINSTBU 61 fields · synced 24 Oct 2026