Primary Device ID | 50382903008662 |
NIH Device Record Key | 4105627e-1f96-463a-a322-77598443d126 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | 300866 |
Catalog Number | 300866 |
Company DUNS | 989811195 |
Company Name | BECTON DICKINSON & COMPANY LTD |
Device Count | 60 |
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 |