Primary Device ID | 07613389540031 |
NIH Device Record Key | ec6a995a-04c9-4610-a9bf-e6cd4afca8d3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sonova Brand (multiple brand) |
Version Model Number | 051-5047-AB |
Company DUNS | 480662550 |
Company Name | Sonova AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613389540031 [Primary] |
QUH | Self-Fitting Air-Conduction Hearing Aid, Over The Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-06-20 |
Device Publish Date | 2022-12-12 |
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