Primary Device ID | 50382903667036 |
NIH Device Record Key | 974a3c82-a9cf-48c8-b931-4906d1ad2c1c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Vacutainer® No Additive |
Version Model Number | 366703 |
Catalog Number | 366703 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 1000 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 00382903667031 [Unit of Use] |
GS1 | 50382903667036 [Primary] |
FMH | CONTAINER, SPECIMEN, STERILE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-07-28 |
50382903667043 | BD Vacutainer® No Additive |
50382903667036 | BD Vacutainer® No Additive |
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 |