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NexTemp 95-2402

by Medical Indicators

NexTemp 95-2402 (NXT Pro F) is a liquid-crystal patient thermometer (FDA Class I; FDA product code FQZ, Thermometer, Clinical Color Change) made by Medical Indicators, listed in FDA GUDID since 17 Nov 2023 (UDI-DI 20016944401425), 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 Number20016944401425 UDI-DI Date17 Nov 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  • Withdrawn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
NexTemp
Generic name
Liquid-crystal patient thermometer, reusable
Model / Ref / Catalog
95-2402, NXT Pro F
Primary DI / UDI-DI
20016944401425
FDA product code
FQZ
GMDN term
Liquid-crystal patient thermometer, reusable
Device class
Class I
Regulation number
880.2900
GUDID distribution status
In Commercial Distribution
Size
Weight — 0.35 Gram

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

  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)