Primary Device ID | 50382903650434 |
NIH Device Record Key | 88d3b5e5-a6cc-473f-b02d-bdf0459b59b6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Vacutainer® |
Version Model Number | 365043 |
Catalog Number | 365043 |
Company DUNS | 225931062 |
Company Name | Becton, Dickinson U.K. Limited |
Device Count | 1000 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382903650439 [Unit of Use] |
GS1 | 50382903650434 [Primary] |
JKA | Tubes, vials, systems, serum separators, blood collection |
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 | 2016-11-04 |
50382903650472 | BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes |
50382903650465 | BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes |
50382903650458 | BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes |
50382903650441 | BD Vacutainer® Barricor™ Lithium Heparin Plasma Tubes |
50382903650434 | BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BD VACUTAINER 78264506 2858038 Live/Registered |
Becton, Dickinson and Company 2003-06-19 |
BD VACUTAINER 77000481 3257557 Dead/Cancelled |
Becton, Dickinson and Company 2006-09-15 |