Savoy QA3 7QA3MXP
by Avante
Savoy QA3 7QA3MXP is a Class II device made by Avante, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00815871020572), registry data as of 22 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 | Number00815871020572 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00815871020572
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Savoy QA3
- Generic name
- Orthopaedic stretcher
- Model / reference
- 7QA3MXP
- Primary DI / UDI-DI
- 00815871020572
- FDA product code
- FPO
- GMDN term
- Orthopaedic stretcher
- Device class
- Class II
- Regulation number
- 880.6910
- GUDID distribution status
- In Commercial Distribution
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