Primary Device ID | 20721902648896 |
NIH Device Record Key | 7b4873bf-d086-4daa-a395-4b776882d7e4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRILLIUM® AFFINITY NT® |
Version Model Number | 95250 |
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 | 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 |
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 | 00721902648892 [Primary] |
GS1 | 20721902648896 [Package] Contains: 00721902648892 Package: PK [2 Units] In Commercial Distribution |
DTZ | OXYGENATOR, CARDIOPULMONARY BYPASS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-22 |
Device Publish Date | 2015-06-19 |
20613994865971 | OXYGENATOR 95215 TRILLIUM AFF 511T 4PK |
20613994375630 | OXYGENATOR 95217 AFFINITY 541T 2PK |
20613994375623 | OXYGENATOR 95216 AFFINITY 541TR 2PK |
20721902648896 | OXYGENATOR 95250 AFFINITY 2PK 511T 541TT |