SchureMed 800-0143
SchureMed 800-0143 is a Class I device made by Schuerch Corporation, listed in FDA GUDID since 14 Apr 2020 (UDI-DI 00810014603353), 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 | Number00810014603353 | Date14 Apr 2020 | StatusListed |
Official records
- AccessGUDID record 00810014603353
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- SchureMed
- Generic name
- Arm procedure positioner, single-use
- Model / reference
- 800-0143
- Primary DI / UDI-DI
- 00810014603353
- FDA product code
- FWZ
- GMDN term
- Arm procedure positioner, single-use
- Device class
- Class I
- Regulation number
- 878.4950
- GUDID distribution status
- In Commercial Distribution
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