Primary Device ID | 00763000596873 |
NIH Device Record Key | 528268f3-7cab-4d65-adfc-fe06383e7349 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | InterStim™ SureScan™ |
Version Model Number | 978A141 |
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 | |
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 |
Length | 41 Centimeter |
Length | 41 Centimeter |
Length | 41 Centimeter |
Length | 41 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000596873 [Primary] |
QON | Implanted electrical device intended for treatment of fecal 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 | 2024-01-30 |
Device Publish Date | 2024-01-22 |
00763000596910 | LEAD 978B128 ISTM SSMRI 4.32MM EMAN GLBL |
00763000596798 | LEAD 978A128 ISTM SSMRI 2.16MM EMAN GLBL |
00763000596873 | LEAD 978A141 ISTM SSMRI 2.16MM EMAN GLBL |
00763000596835 | LEAD 978A133 ISTM SSMRI 2.16MM EMAN GLBL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() INTERSTIM 74469362 2072076 Live/Registered |
Medtronic, Inc. 1993-12-13 |