Subtilis Luxationshebel mit 22 mm, 31 cm Kunststoffgriff
by Accuratus AG
Ref 36.60.03
Active
CE MDR CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberB-07640229290429 07640229290429 | Date1 May 2026 | StatusActive |
| European Union | CE/MDD | NumberB-07640229290429 07640229290429 | Date1 May 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Model / Reference
- 36.60.03
- Primary DI / UDI-DI
- 07640229290429
- Basic UDI-DI
- B-07640229290429, 0764022929PG0136RZ
- Direct Marketing DI
- 07640229290429
- EMDN Code
- L0399 General surgery instruments, reusable - other
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CH-MF-000018336
- Authorised representative
- Accuratus UG DE-AR-000026461
Other devices from Accuratus AG
Properties
Other properties (12)
- Sterile: No
- Implantable: 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