Primary Device ID | 00763000236526 |
NIH Device Record Key | ab4f2eff-abc6-4ebd-9edb-2e1178d23428 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bio-Console® |
Version Model Number | 560BCS1 |
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 |
Storage Environment Atmospheric Pressure | Between 70 KiloPascal and 106 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000236526 [Primary] |
DWA | Control, pump speed, cardiopulmonary bypass |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-23 |
Device Publish Date | 2019-12-14 |
00613994450463 | CONSOLE 560BCS1 CONTROLLER W/SAFETY BRD |
00613994450456 | CONSOLE E560BCS1 EVAL CONTROLLER |
00613994450326 | CONSOLE 560BC1 CONTROLLER W/O SAFETY BRD |
00613994450319 | CONSOLE R560BCS1 REFURB CONTROLLER |
00763000135447 | CONSOLE 560BCS1 CONTROL W/SAFETY MEE NR |
00763000236540 | REFURB CONSOL R560BCS1 W/S BRD 7L NR EMC |
00763000236533 | EVAL CONSOLE E560BCS1 W/S BRD 7L NR EMC |
00763000236526 | CONSOLE 560BCS1 W/SAFETY BRD 7L NR EMC |
00763000167325 | CONSOLE 560BCS1 CONTROL W/SAFETY BRD MEE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BIO-CONSOLE 73074881 1045350 Live/Registered |
BIO-MEDICUS, INC. 1976-01-21 |