KLS Martin
by KLS Martin SE & Co. KG 72 variants
Ref 53-800-17-04
Active
CE MDR
Valid until
7 May 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number40576052935T 04057605895599 | Date30 Jul 2026 | StatusActive |
Certificates
- 20452GB450250508 Active
Technical documentation EU MDR
- Certifier
- DNV MEDCERT GmbH 0482
- Issued
- 8 May 2025
- Expires
- 7 May 2030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Absorbable implants Mg
- Model / Reference
- 53-800-17-04
- Primary DI / UDI-DI
- 04057605895599
- Basic UDI-DI
- 40576052935T
- EMDN Code
- P09120606 Osteosynthesis devices, biodegradable screws and bars
- Device Class
- Class III
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000005551
From the manufacturer
Manufacturer's product page: Art.-Nr. 80-042-00-04 maXium® m-Version mit Buchsenmodul für KLS Martin-Zubehör
Other devices from KLS Martin SE & Co. KG
Properties
Other properties (11)
- Reusable: No
- Contains Latex: No
- Reprocessed: 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