Primary Device ID | 00613994100894 |
NIH Device Record Key | e21d86d9-77fe-48aa-a399-bab1008c27b3 |
Commercial Distribution Discontinuation | 2018-08-13 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 7440-48 |
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 | 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 |
Length | 122 Centimeter |
Length | 122 Centimeter |
Length | 122 Centimeter |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Length | 48 Inch |
Length | 122 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00613994100894 [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 | 2018-10-22 |
Device Publish Date | 2014-09-23 |
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