Primary Device ID | 00885074200330 |
NIH Device Record Key | c59f51e9-b06c-4bd9-a826-77294759dcd8 |
Commercial Distribution Discontinuation | 2018-08-13 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 355032 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00885074200330 [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 |
00763000963705 - NA | 2024-08-05 CUSTOM PACK BB11W58R3 BAP SOUTH E C |
00763000964061 - NA | 2024-08-05 CUSTOM PACK BB12H45R ST BERNARDS SU |
20763000963723 - NA | 2024-08-02 CUSTOM PACK 12F80R1 10PK 3/8 PLUG |
00763000963736 - NA | 2024-08-02 CUSTOM PACK CB5D50R5 3/8 A-V |
20763000963754 - NA | 2024-08-02 CUSTOM PACK 12H75R 10PK GUARDIA TUBING G |
00763000963781 - NA | 2024-08-02 CUSTOM PACK BB7L12R8 ADULT E |
00763000926465 - Hancock™ 150 | 2024-07-30 HANCOCK VALVED CONDUIT MO 12MM |
00763000926472 - Hancock™ 150 | 2024-07-30 HANCOCK VALVED CONDUIT MO 14MM |