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physIQ Patient Kit Model K

by Physiq, Inc

physIQ Patient Kit Model K is a device made by Physiq, Inc, listed in FDA GUDID since 26 Jul 2021 (UDI-DI 00850023120083), 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 Number00850023120083 UDI-DI Date26 Jul 2021ListedStatusListed 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  • Withdrawn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 Patient Kit
Generic name
Electrocardiography telemetric monitoring system
Model / reference
Model K
Primary DI / UDI-DI
00850023120083
GMDN term
Electrocardiography telemetric monitoring system
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Electrocardiography telemetric monitoring system

Other devices from Physiq, Inc

See all devices from Physiq, Inc →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)