113-209-4540S
by Biedermann Motech GmbH & Co. KG
Ref 113-209-4540SModel MOSS Family
Active
CE MDR
Valid until
6 Dec 2028
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number42508696000010009E 04255772606189 | Date15 Jul 2026 | StatusActive |
Certificates
- 1000319809 Active
Technical documentation EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 7 Jul 2026
- Expires
- 6 Jul 2031
- 1000319811 Active
Quality management system EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 7 Jul 2026
- Expires
- 6 Dec 2028
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- MOSS Family, 113-209-4540S
- Primary DI / UDI-DI
- 04255772606189
- Basic UDI-DI
- 42508696000010009E
- EMDN Code
- P09070302 Thoracolumbosacral fixation systems
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000005455
Other devices from Biedermann Motech GmbH & Co. KG
Properties
Other properties (12)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Sutures: 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