Primary Device ID | EGOL840940 |
NIH Device Record Key | 70664634-e1e6-4a46-aec8-316838296160 |
Commercial Distribution Discontinuation | 2024-05-26 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | PHONAK |
Version Model Number | C&C Wipe |
Company DUNS | 328465042 |
Company Name | Egger Otoplastik + Labortechnik GmbH |
Device Count | 25 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EGOL840851 [Primary] |
HIBCC | EGOL840940 [Unit of Use] |
LRJ | Disinfectant, Medical Devices |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-09-27 |
Device Publish Date | 2023-01-01 |
EGOL840940 - PHONAK | 2024-09-27 |
EGOL840940 - PHONAK | 2024-09-27 |
EGOL206001 - egger | 2022-09-08 |
EGOL206030 - egger | 2022-09-08 |
EGOL206190 - egger | 2022-09-08 |
EGOL207001 - egger | 2022-09-08 |
EGOL207021 - egger | 2022-09-08 |
EGOL207031 - egger | 2022-09-08 |
EGOL207041 - egger | 2022-09-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PHONAK 87580091 5428357 Live/Registered |
Sonova AG 2017-08-23 |
PHONAK 79084308 3972695 Live/Registered |
Sonova AG 2010-03-09 |
PHONAK 75808854 2389792 Live/Registered |
SONOVA AG 1999-09-23 |
PHONAK 73521367 1389790 Dead/Cancelled |
PHONAK AG 1985-02-08 |
PHONAK 71552851 0543910 Dead/Cancelled |
A. G. FUR ELEKTRO-AKUSTIK 1948-03-24 |