Primary Device ID | 00721902309588 |
NIH Device Record Key | 6f9302d1-4f69-460f-891b-2385c8366455 |
Commercial Distribution Discontinuation | 2019-01-25 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 5436 |
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 | 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 |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00721902309588 [Primary] |
NVZ | Pulse generator, permanent, implantable |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00721902309588]
Moist Heat or Steam Sterilization;Ethylene Oxide
[00721902309588]
Moist Heat or Steam Sterilization;Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-18 |
Device Publish Date | 2014-09-23 |
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