Ortéza ramenního kloubu Desault, vel.X0, černá
Ref Desault
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number859404276024JK | Date8 Sep 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Trade Name
- Ortéza ramenního kloubu Desault, vel.X0, černáOrtéza ramenního kloubu Desault, vel.0, černáOrtéza ramenního kloubu Desault, vel.3, černáOrtéza ramenního kloubu Desault, vel.1, černáOrtéza ramenního kloubu Desault, vel.2, černá
- Device Name
- Ortéza ramenního kloubu Desault
- Model / Reference
- Desault
- Primary DI / UDI-DI
- 08594042762795, 08594042762788, 08594042762375, 08594042762351, 08594042762368
- Basic UDI-DI
- 859404276024JK
- EMDN Code
- Y060621 Shoulder orthoses
- Device Class
- Class I
- EU market of registration
- Czechia
Manufacturer details
- EUDAMED SRN
- CZ-MF-000001007
Other devices from HANDICAP, a.s.
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- 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