Primary Device ID | 00850023296009 |
NIH Device Record Key | 603b9c2e-c50c-49cf-8086-24c86eaa36ad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MyNotifi Rx |
Version Model Number | Version 2 |
Catalog Number | MyNotifi RX - large |
Company DUNS | 107660874 |
Company Name | MEDHAB, 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 | true |
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 | false |
OTC Over-The-Counter | false |