Primary Device ID | 06934325338705 |
NIH Device Record Key | c6b86c44-e514-4d77-81b5-eb9d4edae35a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Portable Mesh Nebulizer |
Version Model Number | Air Pro VIII |
Company DUNS | 544431678 |
Company Name | FEELLIFE HEALTH 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 | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |