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NexTemp 8500

by Medical Indicators

NexTemp 8500 (NXT GO F) is a Class I device made by Medical Indicators, listed in FDA GUDID since 29 Aug 2024 (UDI-DI 00016944401438), 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 Number00016944401438 UDI-DI Date29 Aug 2024ListedStatusListed 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  • Withdrawn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
8500, NXT GO F
Primary DI / UDI-DI
00016944401438
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 — 0.23 Gram

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
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)