Primary Device ID | 07613389770872 |
NIH Device Record Key | 689089c9-c2b7-4ec1-b52b-1404f864fd0e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ampli-power I 5 5P ITE-R WL PH |
Version Model Number | R WL PH |
Catalog Number | 063-0526-0167 |
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 | 07613389770872 [Primary] |
OSM | Hearing Aid, Air-Conduction With Wireless Technology, 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 | 2024-11-19 |
Device Publish Date | 2024-11-11 |
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