Primary Device ID | 00817365021539 |
NIH Device Record Key | 1c0ba57a-848b-456c-88f2-2c39d93a581d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Salute RDX |
Version Model Number | FC-MOX0032 |
Catalog Number | FC-MOX0032 |
Company DUNS | 958807575 |
Company Name | MOXI ENTERPRISES, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 |