Medtronic

GUDID 00763000917784

AEX GENERATOR 40-405-1 US

MEDTRONIC, INC.

Electrosurgical system generator
Primary Device ID00763000917784
NIH Device Record Key5ce880de-e620-4fb0-b08f-49e737c69ac6
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedtronic
Version Model Number40-405-1
Company DUNS030200852
Company NameMEDTRONIC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000917784 [Primary]

FDA Product Code

GEIElectrosurgical, cutting & coagulation & accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-10-28
Device Publish Date2024-10-19

On-Brand Devices [Medtronic]

00763000917784AEX GENERATOR 40-405-1 US
00763000281014AEX GENERATOR 40-405-1 CHINA

Trademark Results [Medtronic]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MEDTRONIC
MEDTRONIC
98303739 not registered Live/Pending
Medtronic, Inc.
2023-12-07
MEDTRONIC
MEDTRONIC
98131172 not registered Live/Pending
Medtronic, Inc.
2023-08-14
MEDTRONIC
MEDTRONIC
97703863 not registered Live/Pending
Medtronic, Inc.
2022-12-05
MEDTRONIC
MEDTRONIC
97699724 not registered Live/Pending
Medtronic, Inc.
2022-12-01
MEDTRONIC
MEDTRONIC
97693235 not registered Live/Pending
Medtronic, Inc.
2022-11-28
MEDTRONIC
MEDTRONIC
97665324 not registered Live/Pending
Medtronic, Inc.
2022-11-07
MEDTRONIC
MEDTRONIC
97157293 not registered Live/Pending
Medtronic, Inc.
2021-12-06
MEDTRONIC
MEDTRONIC
90156891 not registered Live/Pending
Medtronic, Inc.
2020-09-03
MEDTRONIC
MEDTRONIC
90144502 not registered Live/Pending
Medtronic, Inc.
2020-08-28
MEDTRONIC
MEDTRONIC
90144494 not registered Live/Pending
Medtronic, Inc.
2020-08-28
MEDTRONIC
MEDTRONIC
90135505 not registered Live/Pending
Medtronic, Inc.
2020-08-25
MEDTRONIC
MEDTRONIC
90062122 not registered Live/Pending
Medtronic, Inc.
2020-07-20

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.