Primary Device ID | 08056600520099 |
NIH Device Record Key | ca5c2ede-0074-4e46-9da9-c19b231b16e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N23 CCD System |
Version Model Number | N23 |
Catalog Number | N2350NAR1 |
Company DUNS | 435743877 |
Company Name | NICAL SPA |
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 | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |