PATIENT TABLE Regular
PATIENT TABLE Regular (S MPRTHD) is a Class II device made by Pausch, L.L.C., listed in FDA GUDID since 27 Jan 2023 (UDI-DI B884SMPRTHD0), 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 | NumberB884SMPRTHD0 | Date27 Jan 2023 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Patient Table
- Generic name
- Basic diagnostic x-ray system table, non-powered
- Model / Ref / Catalog
- Regular, S MPRTHD
- Primary DI / UDI-DI
- B884SMPRTHD0
- FDA product code
- IXQ, IXR
- GMDN term
- Basic diagnostic x-ray system table, non-powered
- Device class
- Class II
- Regulation number
- 892.1980
- GUDID distribution status
- In Commercial Distribution
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