Primary Device ID | 00681490148450 |
NIH Device Record Key | 38cfc650-c79e-4620-b80b-7fbc03e1f3ab |
Commercial Distribution Discontinuation | 2018-05-02 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 6707-35 |
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 | 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 |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Length | 35 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00681490148450 [Primary] |
DTB | permanent pacemaker Electrode |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-08-13 |
Device Publish Date | 2014-09-23 |
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