Primary Device ID | 50382903664448 |
NIH Device Record Key | 10c3d601-1cc1-4501-8489-e45cb4d0d84a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Vacutainer® SST™ II Advance |
Version Model Number | 366444 |
Catalog Number | 366444 |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382903664443 [Unit of Use] |
GS1 | 50382903664448 [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 | 2016-07-28 |
50382903679572 | BD Vacutainer® SST™ II Advance |
50382903679558 | BD Vacutainer® SST™ II Advance |
50382903679534 | BD Vacutainer® SST™ II Advance |
50382903668828 | BD Vacutainer® SST™ II Advance |
50382903664448 | BD Vacutainer® SST™ II Advance |
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 |