Primary Device ID | 00673978169880 |
NIH Device Record Key | db785df5-9709-47a9-80f3-5ca350f856d0 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | E95183-01 |
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 | true |
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 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00673978169880 [Primary] |
DWA | Control, pump speed, cardiopulmonary bypass |
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 | 2015-06-19 |
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00763000897697 - Launcher™ | 2024-05-15 CATHETER LA6HSIA LA 6F 110CM HSI |
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00763000897710 - Launcher™ | 2024-05-15 CATHETER LA6JCL40A LA 6F 110CM JCL40 |