Protekt PMFEBHR
Protekt PMFEBHR is a Class II device made by Proactive Medical Products, listed in FDA GUDID since 23 Nov 2022 (UDI-DI 05060488574009), 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 | Number05060488574009 | Date23 Nov 2022 | StatusListed |
Official records
- AccessGUDID record 05060488574009
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Protekt
- Generic name
- Basic electric home bed
- Model / Ref / Catalog
- PMFEBHR
- Primary DI / UDI-DI
- 05060488574009
- FDA product code
- FNL
- GMDN term
- Basic electric home bed
- Device class
- Class II
- Regulation number
- 880.5100
- GUDID distribution status
- In Commercial Distribution
- Size
- Height — 24 InchLength — 80 InchWidth — 36 Inch
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