Primary Device ID | EADF025381950733217201 |
NIH Device Record Key | 18b7f550-61cb-4e93-8db1-a0c45334eb84 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | audifon |
Version Model Number | sueno pro R |
Catalog Number | 025381-9507-332-1720 |
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 | EADF025381950733217201 [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 |