Primary Device ID | 00681490026901 |
NIH Device Record Key | 489d563f-2a57-445d-a73c-945dcbc7e198 |
Commercial Distribution Discontinuation | 2019-04-10 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 080118 |
Company DUNS | 006261481 |
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 | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00681490026901 [Primary] |
KFJ | Materials, repair or replacement, pacemaker |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-05-07 |
Device Publish Date | 2014-09-23 |
00763000959067 - NA | 2024-07-02 CUSTOM PACK BB5348R24 PHOEBE P |
20763000959818 - NA | 2024-07-02 CUSTOM PACK BB12G18R1 10PK EXTRA CPG LN |
00763000957544 - NA | 2024-06-28 CUSTOM PACK BB7J30R4 LIV SHUNT |
00763000957551 - NA | 2024-06-28 CUSTOM PACK BBB7S09R13 SUPPRT SM |
20763000957760 - NA | 2024-06-28 CUSTOM PACK BB12G13R 5PK FL MEM MANIFOL |
00763000957780 - NA | 2024-06-28 CUSTOM PACK 11H88R7 ACCESSORY PACK |
00763000958015 - NA | 2024-06-28 CUSTOM PACK HY11R06R2 SUPP 1/4 PK |
20763000958033 - NA | 2024-06-28 CUSTOM PACK BB9B82R2 5PK JUMP PACK |