| Primary Device ID | 06973810850339 |
| NIH Device Record Key | d30e798e-a9f7-47a9-810d-f787a372338c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Na |
| Version Model Number | FC7108 |
| Company DUNS | 560082555 |
| Company Name | Shenzhen Jian Feng Electronic Technology Co., Ltd. |
| Device Count | 1 |
| 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 | false |
| Manufacturing Date | false |
| 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 | 06973810850339 [Primary] |
| GS1 | 16973810850336 [Package] Package: [60 Units] In Commercial Distribution |
| GS1 | 26973810850333 [Package] Package: [40 Units] In Commercial Distribution |
| NGX | Stimulator, Muscle, Powered, For Muscle Conditioning |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-08-16 |
| Device Publish Date | 2024-08-08 |
| 16973810850404 - AVCOO | 2024-12-23 |
| 16973810850398 - AUVON | 2024-11-11 |
| 16973810850374 - No | 2024-09-12 |
| 16973810850350 - No | 2024-08-29 |
| 16973810850367 - No | 2024-08-29 |
| 16973810850343 - No | 2024-08-21 |
| 06973810850339 - Na | 2024-08-16 |
| 06973810850339 - Na | 2024-08-16 |
| 16973810850312 - No | 2024-07-24 |