Primary Device ID | 04049471100037 |
NIH Device Record Key | cc055998-6630-4880-8afc-1ec24ba594a0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FORUM ASSIST match |
Version Model Number | 1.4.1 |
Company DUNS | 314594680 |
Company Name | Carl Zeiss Meditec AG |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |