Primary Device ID | 06974308960271 |
NIH Device Record Key | a8e0b58e-8af2-4a78-ab96-fbee007bead9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Retone |
Version Model Number | Clear 102H |
Company DUNS | 544329913 |
Company Name | Xiamen Retone Hearing Technology Co., Ltd. |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06974308960271 [Primary] |
ESD | Hearing Aid, Air-Conduction, Prescription |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-03 |
Device Publish Date | 2025-01-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() RETONE 97193401 not registered Live/Pending |
Xiamen Retone Hearing Technology Co., Ltd. 2021-12-28 |
![]() RETONE 87103587 5449154 Live/Registered |
RESTORATION DERMACARE LLC 2016-07-14 |