Primary Device ID | 20721902325780 |
NIH Device Record Key | 5abaf15f-b5a6-4ade-be92-b63e4d932b27 |
Commercial Distribution Discontinuation | 2017-11-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | TRILLIUM™ Bio-Probe® |
Version Model Number | DP38PT |
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 | false |
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 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00721902325786 [Primary] |
GS1 | 20721902325780 [Package] Contains: 00721902325786 Package: PK [10 Units] Discontinued: 2017-11-30 Not in Commercial Distribution |
DPT | PROBE, BLOOD-FLOW, EXTRAVASCULAR |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-06-16 |
20721902325780 | PROBE DP38PT TRILLIUM BIO 1/4 |
20721902325742 | PROBE DP38T TRILLIUM BIO-PROBE ADULT10PK |