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Ds6

FDA UDI

Class II (US FDA UDI)

by Foresite Healthcare, Llc

Identity

Trade Name
DS6 FDA UDI
Generic Name
Bed/chair occupant movement pressure/vibration sensor FDA UDI
Device Name
Depth Sensor FDA UDI
Model / Reference
DS6-UB FDA UDI
Description
Depth Sensor FDA UDI

Identifiers

Primary DI / UDI-DI
00850064651041 FDA UDI
FDA Product Code
ISD FDA UDI
GMDN Term
Bed/chair occupant movement pressure/vibration sensor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5360 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bed/chair occupant movement pressure/vibration sensor

Ds6 by Foresite Healthcare, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed/chair occupant movement pressure/vibration sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Foresite Healthcare, Llc

Sources (1)

  • FDA UDI c8562739-5ed2-4074-a473-4bc4d0e34982 35 fields · synced Jun 8, 2026