Primary Device ID | 00613994842336 |
NIH Device Record Key | 834d2b84-061d-4767-ab64-d335e7341909 |
Commercial Distribution Discontinuation | 2018-08-13 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | RestoreULTRA™ |
Version Model Number | 37712 |
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 | true |
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 |
Storage Environment Temperature | Between 0 Degrees Fahrenheit and 126 Degrees Fahrenheit |
Storage Environment Temperature | Between 0 Degrees Fahrenheit and 126 Degrees Fahrenheit |
Storage Environment Temperature | Between 0 Degrees Fahrenheit and 126 Degrees Fahrenheit |
Storage Environment Temperature | Between 0 Degrees Fahrenheit and 126 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00613994842336 [Primary] |
LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-10-02 |
Device Publish Date | 2014-09-23 |
00613994842343 | INS 37712 RESTOREULTRA eMAN BLU WRNCH US |
00613994842336 | INS 37712 RESTORE ULTRA BLUE WRENCH US |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RESTOREULTRA 78903139 3433265 Live/Registered |
Medtronic, Inc. 2006-06-07 |