Primary Device ID | 00763000344504 |
NIH Device Record Key | b0a9c517-3ef6-4688-9e2b-fd01058b8aea |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | CB8B11R7 |
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 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000344504 [Primary] |
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 | 2020-01-06 |
Device Publish Date | 2019-12-29 |
20763000974996 - NA | 2024-09-17 CUSTOM PACK BB11J93R1 5PK OMCE |
20763000975016 - NA | 2024-09-17 CUSTOM PACK BB10M39R3 10PK VAMP/ACC |
00763000975197 - NA | 2024-09-17 CUSTOM PACK BB8G55R17 A PACK |
00763000974190 - NA | 2024-09-16 CUSTOM PACK HY9L80R7 SADT FUS |
00763000974251 - NA | 2024-09-16 CUSTOM PACK HY4D49R18 LEFT HBY |
00763000975135 - NA | 2024-09-16 CUSTOM PACK BB12G92R4 L PEDI/S ADUL |
00763000974572 - NA | 2024-09-10 CUSTOM PACK BB3X42R20 UNV |
20763000181080 - NA | 2024-09-09 CABLE 5833SL SURGICAL5PK DISP |