Primary Device ID | 00310119043288 |
NIH Device Record Key | 25daacab-5cb1-4c05-8343-48ef2a6d64c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bausch & Lomb |
Version Model Number | 624328 |
Catalog Number | FCP-4360 |
Company DUNS | 196603781 |
Company Name | Bausch & Lomb Incorporated |
Device Count | 1 |
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 | 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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |