Mx-Pro 6083
Mx-Pro 6083 (6083-000-000) is a Class II device made by Stryker Corp., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07613327261585), 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 | Number07613327261585 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 07613327261585
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Mx-Pro
- Generic name
- Ambulance stretcher, manual
- Model / Ref / Catalog
- 6083, 6083-000-000
- Primary DI / UDI-DI
- 07613327261585
- FDA product code
- FPO
- GMDN term
- Ambulance stretcher, manual
- Device class
- Class II
- Regulation number
- 880.6910
- GUDID distribution status
- In Commercial Distribution
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