Primary Device ID | 06973375880390 |
NIH Device Record Key | 4359bdf8-1448-4ffc-ae25-939e4b44811e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AcoSound |
Version Model Number | Celesto-BTE-P |
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 | 06973375880390 [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 | 2022-11-17 |
Device Publish Date | 2022-11-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACOSOUND 87736474 not registered Live/Pending |
Hangzhou Acosound Technology Co.,Ltd. 2017-12-28 |