Skip to content

Mutars®

by implantcast GmbH 252 variants

Ref 52200001Model MUTHUENDPUNC

Mutars® (52200001) is a Class III device made by implantcast GmbH, registered in EUDAMED on 21 Jul 2026 (Basic UDI-DI 4048844MUTHUENDPUNCKE) with CE/MDR certificate 13266GB450221104 valid until 3 Nov 2027, active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4048844MUTHUENDPUNCKE Basic UDI-DI 04048844044541UDI-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 4048844MUTHUENDPUNCKE
  3. Certificate expires EUDAMED 13266GB450221104

Coverage

1 jurisdiction

GermanyPoland
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Expiring

  • Germany
  • Poland

Specification

EUDAMED

Model / reference
MUTHUENDPUNC, 52200001
Primary DI / UDI-DI
04048844044541
Basic UDI-DI
4048844MUTHUENDPUNCKE
EMDN code
P0901040299 Diaphysary humeral components - other
Device class
Class III
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000010002

Similar devices in this category

Other devices filed under DIAPHYSARY HUMERAL COMPONENTS.

Other devices from implantcast GmbH

See all devices from implantcast GmbH →

Properties

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