Primary Device ID | 00643169878167 |
NIH Device Record Key | 89611d97-7d79-4dbb-9104-c60b53809a32 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | R95184-01 |
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 | 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 | false |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Immerse |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Immerse |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Immerse |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Immerse |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Immerse |
Special Storage Condition, Specify | Between 0 and 0 *Do Not Immerse |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169878167 [Primary] |
DPT | PROBE, BLOOD-FLOW, EXTRAVASCULAR |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-02-13 |
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