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Patient Response Unit PRU

by Medoc Corp.

Patient Response Unit PRU (AS 00243) is a thermotester (FDA Class I; FDA product code LQW, Test, Temperature Discrimination) made by Medoc Corp., listed in FDA GUDID since 20 Jun 2023 (UDI-DI 07290103039264), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290103039264 UDI-DI Date20 Jun 2023ListedStatusListed 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  • Withdrawn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
Patient Response Unit
Generic name
Thermotester, diagnostic
Model / Ref / Catalog
PRU, AS 00243
Primary DI / UDI-DI
07290103039264
FDA product code
LQW
GMDN term
Thermotester, diagnostic
Device class
Class I
Regulation number
882.1200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Thermotester, diagnostic

Similar devices

Other devices filed under FDA product code LQW (Test, Temperature Discrimination).

Other devices from Medoc Corp.

See all devices from Medoc Corp. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)