Sprint 200 1ES200-7
Sprint 200 1ES200-7 is a Class II device made by L I N E T spol. s r.o., listed in FDA GUDID since 10 Nov 2022 (UDI-DI 08592654358467), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08592654358467 | Date10 Nov 2022 | StatusListed |
Official records
- AccessGUDID record 08592654358467
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Sprint 200
- Generic name
- Patient transfer system, manual
- Model / reference
- 1ES200-7
- Primary DI / UDI-DI
- 08592654358467
- FDA product code
- FPO
- GMDN term
- Patient transfer system, manual
- Device class
- Class II
- Regulation number
- 880.6910
- GUDID distribution status
- In Commercial Distribution
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