Bed4 Bed4-RPS
by Foresite Healthcare, LLC 2 variants
Bed4 Bed4-RPS is a Class I device made by Foresite Healthcare, LLC, listed in FDA GUDID since 24 May 2024 (UDI-DI 00850064651089), 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 | Number00850064651089 | Date24 May 2024 | StatusListed |
Official records
- AccessGUDID record 00850064651089
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Bed4
- Generic name
- Bed/chair occupant movement pressure/vibration sensor
- Model / reference
- Bed4-RPS
- Primary DI / UDI-DI
- 00850064651089
- FDA product code
- KMI
- GMDN term
- Bed/chair occupant movement pressure/vibration sensor
- Device class
- Class I
- Regulation number
- 880.2400
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code KMI (Monitor, Bed Patient).
- BED PATIENT PRESENCE MONITOR by Human Technologies, Inc.
- STA-PUT by Design Technologies, Inc.
- ALERT BED ALARM SYSTEM by Alertronics, Inc.
- BARTRONIX IN-BED ACTIVITY MONITOR by Bartronix
- EXIT ALARM by Alertcare
- RSVP RF-2000 by Tactilitics, Inc.
- MONITOR, BED, TECHNOLICS by Technolics, Inc.
- FALL-SAFE VEST by Fsm Corp.
- TELETOM by Berchtold Holding GmbH
- VIVATRAK by Wireless Medcare, LLC