| Primary Device ID | 00763000281014 |
| NIH Device Record Key | 771c43d4-9a23-41cd-a9a0-f7a17b2b1870 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Medtronic |
| Version Model Number | 40-405-1 |
| Company DUNS | 030200852 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000281014 [Primary] |
| GEI | Electrosurgical, cutting & coagulation & accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-10-15 |
| Device Publish Date | 2024-10-07 |
| 00763000917784 | AEX GENERATOR 40-405-1 US |
| 00763000281014 | AEX GENERATOR 40-405-1 CHINA |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEDTRONIC 98303739 not registered Live/Pending |
Medtronic, Inc. 2023-12-07 |
![]() MEDTRONIC 98131172 not registered Live/Pending |
Medtronic, Inc. 2023-08-14 |
![]() MEDTRONIC 97703863 not registered Live/Pending |
Medtronic, Inc. 2022-12-05 |
![]() MEDTRONIC 97699724 not registered Live/Pending |
Medtronic, Inc. 2022-12-01 |
![]() MEDTRONIC 97693235 not registered Live/Pending |
Medtronic, Inc. 2022-11-28 |
![]() MEDTRONIC 97665324 not registered Live/Pending |
Medtronic, Inc. 2022-11-07 |
![]() MEDTRONIC 97157293 not registered Live/Pending |
Medtronic, Inc. 2021-12-06 |
![]() MEDTRONIC 90156891 not registered Live/Pending |
Medtronic, Inc. 2020-09-03 |
![]() MEDTRONIC 90144502 not registered Live/Pending |
Medtronic, Inc. 2020-08-28 |
![]() MEDTRONIC 90144494 not registered Live/Pending |
Medtronic, Inc. 2020-08-28 |
![]() MEDTRONIC 90135505 not registered Live/Pending |
Medtronic, Inc. 2020-08-25 |
![]() MEDTRONIC 90062122 not registered Live/Pending |
Medtronic, Inc. 2020-07-20 |