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Ampmed AMP2402W

by Amplim, LLC

Ampmed AMP2402W is a Class II device made by Amplim, LLC, listed in FDA GUDID since 28 Mar 2025 (UDI-DI 00810477026096), 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 Number00810477026096 UDI-DI Date28 Mar 2025ListedStatusListed 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  • Withdrawn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
Ampmed
Generic name
Intermittent electronic patient thermometer
Model / reference
AMP2402W
Primary DI / UDI-DI
00810477026096
FDA product code
FLL
GMDN term
Intermittent electronic patient thermometer
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

Related devices

Category: Intermittent electronic patient thermometer

Similar devices in this category

Other devices filed under Intermittent electronic patient thermometer.

Other devices from Amplim, LLC

See all devices from Amplim, LLC →

Properties

  • Lot / batch number
  • Manufacturing date
Other properties (13, all answered No)