Skip to content

physIQ Cloud Platform 3.2 (Deneb)

by Physiq, Inc

physIQ Cloud Platform 3.2 (Deneb) is a Class I device made by Physiq, Inc, listed in FDA GUDID since 10 Oct 2020 (UDI-DI 00860004366225), 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 Number00860004366225 UDI-DI Date10 Oct 2020ListedStatusListed 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  • Withdrawn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
physIQ Cloud Platform
Generic name
Electrocardiography telemetric monitoring system
Model / reference
3.2 (Deneb)
Primary DI / UDI-DI
00860004366225
FDA product code
OUG
GMDN term
Electrocardiography telemetric monitoring system
Device class
Class I
Regulation number
880.6310
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code OUG (Medical Device Data System).

Other devices from Physiq, Inc

See all devices from Physiq, Inc →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)