| Primary Device ID | EADF025381950731317201 |
| NIH Device Record Key | 8aff8911-1c2f-45b8-9493-464b992da1a1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | audifon |
| Version Model Number | sueno pro R |
| Catalog Number | 025381-9507-313-1720 |
| 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 | EADF025381950731317201 [Primary] |
| KLW | Masker, Tinnitus |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-18 |
| Device Publish Date | 2019-03-08 |
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 |