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Bed4 Bed4-UB

by Foresite Healthcare, LLC

Bed4 Bed4-UB is a Class I device made by Foresite Healthcare, LLC, listed in FDA GUDID since 24 May 2024 (UDI-DI 00850064651072), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850064651072 UDI-DI Date24 May 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Bed4
Generic name
Bed/chair occupant movement pressure/vibration sensor
Model / reference
Bed4-UB
Primary DI / UDI-DI
00850064651072
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).

Other devices from Foresite Healthcare, LLC

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Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)