| Primary Device ID | 00763000203801 |
| NIH Device Record Key | 9fc8569c-d479-4b9b-8825-fa635e435fb9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InterStim™ SureScan™ |
| Version Model Number | 978B141 |
| Company DUNS | 796986144 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| 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 |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Length | 41 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000203801 [Primary] |
| EZW | Stimulator, electrical, implantable, for incontinence |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-08-18 |
| Device Publish Date | 2020-08-10 |
| 00763000203801 | LEAD 978B141 ISTM SSMRI 4.32MM EMAN US |
| 00763000203764 | LEAD 978B133 ISTM SSMRI 4.32MM EMAN US |
| 00763000203726 | LEAD 978B128 ISTM SSMRI 4.32MM EMAN US |
| 00763000203689 | LEAD 978A141 ISTM SSMRI 2.16MM EMAN US |
| 00763000203641 | LEAD 978A133 ISTM SSMRI 2.16MM EMAN US |
| 00763000203603 | LEAD 978A128 ISTM SSMRI 2.16MM EMAN US |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() INTERSTIM 74469362 2072076 Live/Registered |
Medtronic, Inc. 1993-12-13 |