Primary Device ID | 00304040003961 |
NIH Device Record Key | d8840db2-6c14-43f5-aeec-7745f9251c60 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Maxicide 28 day |
Version Model Number | 1026003 |
Catalog Number | 1026003 |
Company DUNS | 012430880 |
Company Name | HENRY SCHEIN, INC. |
Device Count | 1 |
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 | false |
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 | false |
OTC Over-The-Counter | false |