Primary Device ID | 20763000358437 |
NIH Device Record Key | f7a881a3-09e1-424c-994c-9f841e9e0537 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 8R92R1 |
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 | 00763000358426 [Primary] |
GS1 | 20763000358437 [Package] Contains: 00763000358426 Package: PK [4 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 | 2020-02-24 |
Device Publish Date | 2020-02-16 |
20763000770291 - TrailBlazer™ | 2024-07-16 PS ASC-014-090 TRAILBLAZER ANGLED V04 |
20763000770307 - TrailBlazer™ | 2024-07-16 PS ASC-014-135 TRAILBLAZER ANGLED V04 |
20763000770314 - TrailBlazer™ | 2024-07-16 PS ASC-014-150 TRAILBLAZER ANGLED V04 |
20763000770321 - TrailBlazer™ | 2024-07-16 PS ASC-018-090 TRAILBLAZER ANGLED V04 |
20763000770338 - TrailBlazer™ | 2024-07-16 PS ASC-018-135 TRAILBLAZER ANGLED V04 |
20763000770345 - TrailBlazer™ | 2024-07-16 PS ASC-018-150 TRAILBLAZER ANGLED V04 |
20763000770352 - TrailBlazer™ | 2024-07-16 PS ASC-035-065 TRAILBLAZER ANGLED V04 |
20763000770369 - TrailBlazer™ | 2024-07-16 PS ASC-035-090 TRAILBLAZER ANGLED V04 |