Primary Device ID | 20763000361383 |
NIH Device Record Key | ae3c6e3f-790c-42be-a919-1b0b7707dda9 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 11F39R |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000361372 [Primary] |
GS1 | 20763000361383 [Package] Contains: 00763000361372 Package: PK [10 Units] In Commercial Distribution |
DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-06 |
Device Publish Date | 2020-02-27 |
00763000902537 - Launcher™ | 2024-06-04 CATHETER LA83DRCD LA 8F 90CM 3DRC |
00763000902544 - Launcher™ | 2024-06-04 CATHETER LA83DRCSH LA 8F 100CM 3DRC |
00763000902551 - Launcher™ | 2024-06-04 CATHETER LA83DRCSHD LA 8F 90CM 3DRC |
00763000902568 - Launcher™ | 2024-06-04 CATHETER LA83DRIGHT LA 8F 100CM 3DRGT |
00763000902575 - Launcher™ | 2024-06-04 CATHETER LA83DRIGHTD LA 8F 90CM 3DRGT |
00763000902582 - Launcher™ | 2024-06-04 CATHETER LA8AL10 LA 8F 100CM AL10 |
00763000902599 - Launcher™ | 2024-06-04 CATHETER LA8AL10D LA 8F 90CM AL10 |
00763000902605 - Launcher™ | 2024-06-04 CATHETER LA8AL10F LA 8F 80CM AL10 |