Primary Device ID | 06973375880086 |
NIH Device Record Key | 7cba15f3-6d9f-43b4-aafa-99606780394f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Acosound |
Version Model Number | W12-BTE-M |
Company DUNS | 542986440 |
Company Name | Hangzhou AcoSound 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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06973375880086 [Primary] |
ESD | Hearing Aid, Air Conduction |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-11-04 |
Device Publish Date | 2021-10-27 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACOSOUND 87736474 not registered Live/Pending |
Hangzhou Acosound Technology Co.,Ltd. 2017-12-28 |