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NexTemp 2112US

by Medical Indicators

NexTemp 2112US (NXT C Regular) is a Class I device made by Medical Indicators, listed in FDA GUDID since 29 May 2021 (UDI-DI 00016944401025), 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 Number00016944401025 UDI-DI Date29 May 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  • Withdrawn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
NexTemp
Generic name
Liquid-crystal patient thermometer, single-use
Model / Ref / Catalog
2112US, NXT C Regular
Description
NexTemp US C Single-use Clinical Thermometer
Primary DI / UDI-DI
00016944401025
FDA product code
FQZ
GMDN term
Liquid-crystal patient thermometer, single-use
Device class
Class I
Regulation number
880.2900
GUDID distribution status
In Commercial Distribution
Size
Weight — 0.00134 Pound

Related devices

Category: Liquid-crystal patient thermometer, single-use

Similar devices

Other devices filed under FDA product code FQZ (Thermometer, Clinical Color Change).

Other devices from Medical Indicators

See all devices from Medical Indicators →

Properties

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