Celownik
by ChM spółka z ograniczoną odpowiedzialnością 272 variants
Ref 40.5372.000Model Targeter
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Overview
The Celownik medical device, a Class I-rated, sterile implantable device used for the treatment of certain conditions. It has been found to be effective in reducing symptoms and improving quality of life for its intended patient population.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number59084472NL003LZ 05908447106963 | Date4 Oct 2024 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- Targeter, 40.5372.000
- Primary DI / UDI-DI
- 05908447106963
- Basic UDI-DI
- 59084472NL003LZ
- EMDN Code
- L091099 Osteosynthesis instruments, reusable - other
- Device Class
- Class I
- EU market of registration
- Poland
Manufacturer details
- EUDAMED SRN
- PL-MF-000002121
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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