| 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 |
| 16945936705296 - METIKO | 2025-09-10 |
| 16945936704886 - AHA Technologies | 2025-02-20 |
| 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 |
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 |