| Primary Device ID | EADF004657295633517201 | 
| NIH Device Record Key | de624034-5f07-480c-afb5-da2acc0acda0 | 
| Commercial Distribution Discontinuation | 2018-12-31 | 
| Commercial Distribution Status | Not in Commercial Distribution | 
| Brand Name | audifon | 
| Version Model Number | arriva M TRT | 
| Catalog Number | 004657-2956-335-1720 | 
| Company DUNS | 344064407 | 
| Company Name | audifon GmbH & Co. KG | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| 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 | 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 | true | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| HIBCC | EADF004657295633517201 [Primary] | 
| KLW | Masker, Tinnitus | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 4 | 
| Public Version Date | 2019-02-22 | 
| Device Publish Date | 2016-11-18 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  AUDIFON  79043076  not registered Dead/Abandoned | Audifon GmbH & Co. KG 2007-05-10 | 
|  AUDIFON  79016369  3154377 Dead/Cancelled | Audifon GmbH & Co. KG 2005-04-11 | 
|  AUDIFON  77980719  3885436 Live/Registered | audifon GmbH & Co. KG 2009-02-17 | 
|  AUDIFON  77671744  not registered Dead/Abandoned | audifon GmbH & Co. KG 2009-02-17 |