Mds
Mds is a Class II device made by Foresite Healthcare, LLC, listed in FDA GUDID since 24 May 2024 (UDI-DI 00850064651027), registry data as of 21 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 | Number00850064651027 | Date24 May 2024 | StatusListed |
Official records
- AccessGUDID record 00850064651027
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Biomechanical function analysis system, motion-tracking
- Model / reference
- MDS
- Primary DI / UDI-DI
- 00850064651027
- FDA product code
- ISD
- GMDN term
- Biomechanical function analysis system, motion-tracking
- Device class
- Class II
- Regulation number
- 890.5360
- GUDID distribution status
- In Commercial Distribution
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