Primary Device ID | 10681490136355 |
NIH Device Record Key | 4d42aec1-e555-4a7a-b012-f696c5ed4084 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 5833S |
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 |
Length | 6 Feet |
Length | 6 Feet |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00681490136358 [Primary] |
GS1 | 10681490136355 [Package] Contains: 00681490136358 Package: PK [5 Units] In Commercial Distribution |
LDF | ELECTRODE, PACEMAKER, TEMPORARY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-06-10 |
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