Primary Device ID | 30382903680406 |
NIH Device Record Key | 26765fb6-28d0-4853-a992-cac4bc44b669 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Vacutainer® Lithium HeparinN Blood Collection Tubes |
Version Model Number | 368040 |
Catalog Number | 368040 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 100 |
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 | 00382903680405 [Unit of Use] |
GS1 | 30382903680406 [Primary] |
GS1 | 50382903680400 [Package] Package: Case [10 Units] In Commercial Distribution |
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 | 4 |
Public Version Date | 2024-04-05 |
Device Publish Date | 2016-07-28 |
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00382906639844 - Horizon | 2024-10-22 CD138 (MI15) BV421 ASR |
00382906651204 - Horizon | 2024-10-22 CD197 (2-L1-A) APC-R700 ASR |
00382906651297 - Horizon | 2024-10-22 CD194 (1G1) BV421 ASR |
00382906651334 - Horizon | 2024-10-22 CD40 (5C3) BV605 ASR |
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 |