Primary Device ID | 00763000188542 |
NIH Device Record Key | 5bf64856-3ab2-411b-8c3d-10e62cfe0fd5 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 05514SP |
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 |
Length | 122 Centimeter |
Handling Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000188542 [Primary] |
DRF | CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-17 |
Device Publish Date | 2019-05-09 |
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