Primary Device ID | 00643169119215 |
NIH Device Record Key | 272f3921-26a7-4ffd-90c5-0ec18ebf5442 |
Commercial Distribution Discontinuation | 2018-08-20 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 37754 |
Company DUNS | 796986144 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169119215 [Primary] |
LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-02-06 |
Device Publish Date | 2014-09-23 |
00763000960308 - NA | 2024-07-09 CUSTOM PACK BB12C30R7 NPR IMC |
00763000960407 - NA | 2024-07-09 CUSTOM PACK BB12G16R3 UCHICAGO CPB |
00763000228699 - NA | 2024-07-08 KIT 20MRK ARCTIC FRNT MANETRACT GLB TIJ |
00763000957193 - NA | 2024-07-08 CUSTOM PACK BB7M46R25 SCV ADLT |
20763000960272 - NA | 2024-07-08 CUSTOM PACK 10R91R5 10PK LRTXBYPS |
20763000960296 - NA | 2024-07-08 CUSTOM PACK SSBB12D06R4 4PK RESOXY BYPA |
00763000879273 - Verify™ | 2024-07-05 ENS 353101 VERIFY ISTM US EMANUAL |
00763000879280 - Verify™ | 2024-07-05 ENS 353101 VERIFY ISTM US REFURB EMAN |