Trialtis 5560-60-0110TS
by Medos International Sàrl GUDID
Listed (no authorization)
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10705034590134 | Date12 Jul 2024 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 23 Oct 2026.
Specification
- Trade Name
- Trialtis
- Generic Name
- Bone-screw internal spinal fixation system rod
- Model / Ref / Catalog
- 5560-60-0110TS, 5560600110TS
- Primary DI / UDI-DI
- 10705034590134
- FDA Product Code
- NKB
- GMDN Term
- Bone-screw internal spinal fixation system rod
- Device Class
- Class II
- Regulation Number
- 888.3070
- Commercial Distribution
- In Commercial Distribution
- MRI Safety
- MR Conditional
Other devices from Medos International SARL
Properties
Other properties (8)
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No