Mutars®
by implantcast GmbH 252 variants
Ref 52101002Model MUTHUGLENUNC
Mutars® (52101002) is a Class III device made by implantcast GmbH, registered in EUDAMED on 21 Jul 2026 (Basic UDI-DI 4048844MUTHUGLENUNCKK) with CE/MDR certificate 13266GB450221104 valid until 3 Nov 2027, active as of 23 Oct 2026.
Expiring
CE MDR
Valid until
3 Nov 2027
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number4048844MUTHUGLENUNCKK 04048844044527 | Date21 Jul 2026 | StatusActive |
Official records
- EUDAMED public site 4048844MUTHUGLENUNCKK
Certificates
- 13266GB450221104 Expiring
Technical documentation EU MDR
- Certifier
- DNV MEDCERT GmbH 0482
- Issued
- 4 Nov 2022
- Expires
- 3 Nov 2027
Timeline
- Certificate issued EUDAMED 13266GB450221104
- Registered EUDAMED 4048844MUTHUGLENUNCKK
- Certificate expires EUDAMED 13266GB450221104
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Expiring
Specification
- Model / reference
- MUTHUGLENUNC, 52101002
- Primary DI / UDI-DI
- 04048844044527
- Basic UDI-DI
- 4048844MUTHUGLENUNCKK
- EMDN code
- P09010303 Glenospheres
- Device class
- Class III
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000010002
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