Primary Device ID | 04560264575387 |
NIH Device Record Key | cd5867f4-885d-464b-882a-73c65ed03093 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FFB-Y |
Version Model Number | FFB-Y |
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 | 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 |