Panama™
Panama™ (08-7000-012) is a Class I device made by Flospine, listed in FDA GUDID since 20 Oct 2021 (UDI-DI B1830870000120), registry data as of 8 Jun 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberB1830870000120 | Date20 Oct 2021 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Internal spinal fixation procedure kit, single-use
- Model / Ref / Catalog
- Panama™, 08-7000-012
- Primary DI / UDI-DI
- B1830870000120
- FDA product code
- LXH
- GMDN term
- Internal spinal fixation procedure kit, single-use
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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