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DS6 DS6-Rp

by Foresite Healthcare, LLC

DS6 DS6-Rp is a Class II device made by Foresite Healthcare, LLC, listed in FDA GUDID since 24 May 2024 (UDI-DI 00850064651058), 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 Number00850064651058 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  • Withdrawn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
DS6
Generic name
Bed/chair occupant movement pressure/vibration sensor
Model / reference
DS6-RP
Primary DI / UDI-DI
00850064651058
FDA product code
ISD
GMDN term
Bed/chair occupant movement pressure/vibration sensor
Device class
Class II
Regulation number
890.5360
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ISD (Exerciser, Measuring).

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Properties

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