Primary Device ID | 20613994697251 |
NIH Device Record Key | 8b46e84b-e476-4d9c-b603-9bc723193ab6 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 304-10POR |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
Device Count | 9 |
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 | false |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Refrigerated 2°C-10°C |
Special Storage Condition, Specify | Between 0 and 0 *Room Temperature 10°C-25°C |
Special Storage Condition, Specify | Between 0 and 0 *Refrigerated 2°C-10°C |
Special Storage Condition, Specify | Between 0 and 0 *Room Temperature 10°C-25°C |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00613994697257 [Unit of Use] |
GS1 | 20613994697251 [Primary] |
JOX | ANALYZER, HEPARIN, AUTOMATED |
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 | 2016-06-13 |
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00763000897680 - Launcher™ | 2024-05-15 CATHETER LA6AL40A LA 6F 110CM AL40 |
00763000897697 - Launcher™ | 2024-05-15 CATHETER LA6HSIA LA 6F 110CM HSI |
00763000897703 - Launcher™ | 2024-05-15 CATHETER LA6HSIIA LA 6F 110CM HSII |
00763000897710 - Launcher™ | 2024-05-15 CATHETER LA6JCL40A LA 6F 110CM JCL40 |