Primary Device ID | 16945936704831 |
NIH Device Record Key | d3288f8b-3676-4fa7-9ba7-5dc2b33ff210 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PowerLix |
Version Model Number | Poco M401 |
Company DUNS | 528181200 |
Company Name | Xiamen New Sound Technology Co., Ltd. |
Device Count | 2 |
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 | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06945936704834 [Primary] |
GS1 | 16945936704831 [Unit of Use] |
ESD | Hearing Aid, Air-Conduction, Prescription |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-19 |
Device Publish Date | 2024-12-11 |
16945936704831 - PowerLix | 2024-12-19 |
16945936704831 - PowerLix | 2024-12-19 |
06945936704742 - Newsound | 2024-12-06 |
06945936704759 - Newsound | 2024-12-06 |
06945936704766 - Newsound | 2024-12-06 |
06945936704773 - Newsound | 2024-12-06 |
06945936704780 - Newsound | 2024-12-06 |
06945936704797 - Newsound | 2024-12-06 |
16945936704060 - Nano | 2024-05-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
POWERLIX 87775579 5555051 Live/Registered |
POWERLIX LTD 2018-01-30 |
POWERLIX 85965213 not registered Dead/Abandoned |
Animal Feed Supplement, Inc. 2013-06-20 |