Primary Device ID | 04560264572836 |
NIH Device Record Key | 01e36f4b-3a3c-4b79-88f8-d7c9a05f2603 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NLX |
Version Model Number | NLX CDE |
Company DUNS | 690710546 |
Company Name | NAKANISHI INC. |
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 | false |
Serial Number | true |
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 |