Primary Device ID | 07613389503647 |
NIH Device Record Key | 544eee42-9259-488a-85db-56135591eaef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IIC Remote Control |
Version Model Number | IIC |
Catalog Number | 054-1005 |
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 | 07613389503647 [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 | 2025-09-30 |
Device Publish Date | 2025-09-22 |
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