Skip to content

Aextm 40-405-1

by Medtronic, Inc. 2 variants

Aextm 40-405-1 is a Class II device made by Medtronic, Inc., listed in FDA GUDID since 25 Apr 2016 (UDI-DI 00643169427013), 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 Number00643169427013 UDI-DI Date25 Apr 2016ListedStatusListed 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  • Withdrawn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
Aextm
Generic name
Electrosurgical system generator
Model / reference
40-405-1
Primary DI / UDI-DI
00643169427013
FDA product code
GEI
GMDN term
Electrosurgical system generator
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrosurgical system generator

Similar devices in this category

Other devices filed under Electrosurgical system generator.

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)