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Mutars®

by implantcast GmbH 252 variants

Ref 52210099Model MUTHUSCONPUNC

Mutars® (52210099) is a Class III device made by implantcast GmbH, registered in EUDAMED on 21 Jul 2026 (Basic UDI-DI 4048844MUTHUSCONPUNCZ6) with CE/MDR certificate 13266GB450221104 valid until 3 Nov 2027, active as of 22 Oct 2026.

Expiring European Union

CE MDR

Valid until

3 Nov 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DNV MEDCERT GmbH

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4048844MUTHUSCONPUNCZ6 Basic UDI-DI 04048844044602UDI-DIDate21 Jul 2026RegisteredStatusActive

Official records

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 13266GB450221104 Expiring Expires in 356 days

    Technical documentation EU MDR

    Certifier
    DNV MEDCERT GmbH 0482
    Issued
    4 Nov 2022
    Expires
    3 Nov 2027

Timeline

3 dated events

  1. Certificate issued EUDAMED 13266GB450221104
  2. Registered EUDAMED 4048844MUTHUSCONPUNCZ6
  3. Certificate expires EUDAMED 13266GB450221104

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Expiring

Specification

EUDAMED

Model / reference
MUTHUSCONPUNC, 52210099
Primary DI / UDI-DI
04048844044602
Basic UDI-DI
4048844MUTHUSCONPUNCZ6
EMDN code
P09018001 Shoulder prostheses fixing screws
Device class
Class III
EU registration type
Standard device
EU market of registration
Norway

Manufacturer details

EUDAMED SRN
DE-MF-000010002

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Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)