Primary Device ID | 00850005614036 |
NIH Device Record Key | e3a38023-d72b-4caf-87f6-e15ea85c6734 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NanoVi |
Version Model Number | NanoVi Pro |
Catalog Number | 4800-00 |
Company DUNS | 016991764 |
Company Name | ENG3 CORPORATION |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850005614036 [Primary] |
KFZ | Humidifier, Non-Direct Patient Interface (Home-Use) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-02-25 |
00850005614067 | NanoVi Exo Wellness |
00850005614050 | NanoVi Exo |
00850005614043 | NanoVi Pro Wellness |
00850005614036 | NanoVi Pro |
00850005614029 | NanoVi Eco Wellness |
00850005614012 | NanoVi Eco |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NANOVI 90251131 not registered Live/Pending |
Jiangming Zheng 2020-10-13 |
NANOVI 87713498 not registered Live/Pending |
Eng3 Corporation 2017-12-08 |