Primary Device ID | EADF0231739045312717201 |
NIH Device Record Key | 3f313f5f-54f4-4476-b6dc-f8ad0d9d1b5c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | audifon |
Version Model Number | rega XS |
Catalog Number | 023173-9045-3127-1720 |
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 | EADF0231739045312717201 [Primary] |
KLW | Masker, Tinnitus |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-05-02 |
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 |