Primary Device ID | 50382903033800 |
NIH Device Record Key | e6014c53-f262-4be4-8c30-070ad5cd1f2b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Vacutainer® Specimen Collection with BD™ Blunt Plastic Cannula |
Version Model Number | 303380 |
Catalog Number | 303380 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 200 |
DM Exempt | true |
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 | 00382903033805 [Unit of Use] |
GS1 | 50382903033800 [Primary] |
FMI | Needle, hypodermic, single lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2016-10-25 |
50382903033800 | BD Vacutainer® Specimen Collection Assembly with BD™ Blunt Plastic Cannula |
00382903033805 | BD Vacutainer® Specimen Collection Assembly with BD™ Blunt Plastic Cannula |
30382903033806 | BD Vacutainer® Specimen Collection Assembly with BD™ Blunt Plastic Cannula |
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 |