Primary Device ID | 05060488903106 |
NIH Device Record Key | 1dd90efc-1047-4ac1-a86f-6d45740b4fa1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Amplivox |
Version Model Number | Ear tips 8-15 mm mushroom |
Company DUNS | 306308354 |
Company Name | Interacoustics A/S |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060488903106 [Primary] |
ETT | Cushion, Earphone (For Audiometric Testing) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2025-06-30 |
Device Publish Date | 2022-12-08 |
05711117027600 | Assortment box Amplivox |
05060488903106 | Ear tips 8-15 mm mushroom |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() AMPLIVOX 85089022 3931020 Live/Registered |
AmpliVox Sound Systems, L.L.C. 2010-07-20 |
![]() AMPLIVOX 77559944 3794009 Live/Registered |
Amplivox Limited 2008-09-02 |
![]() AMPLIVOX 72329213 0914009 Dead/Expired |
AMPLIVOX LIMITED 1969-06-05 |