Bederní pás 100G, v.26cm, vel.5, bílá
Ref 100G
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 | Number859404276018JQ | Date2 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- Withdrawn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
- Bederní pás 100G,v.26cm,vel.5,bíláBederní pás 100G,v.26cm,vel.2,bíláBederní pás 100G,v.26cm,vel.4,bíláBederní pás 100G,v.26cm,vel.1,bíláBederní pás 100G,v.26cm,vel.3,bílá
- Device Name
- Bederní pás 100G
- Model / Reference
- 100G
- Primary DI / UDI-DI
- 08594042760982, 08594042760951, 08594042760975, 08594042760944, 08594042760968
- Basic UDI-DI
- 859404276018JQ
- EMDN Code
- Y060308 Lumbosacral spine 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