| Primary Device ID | 16978146200015 |
| NIH Device Record Key | ca74cee1-2bf8-4526-b248-dd3c4f90c13b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sinrel |
| Version Model Number | YF1503X |
| Company DUNS | 618769254 |
| Company Name | SHENZHEN SINREL TECH LTD |
| 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 | false |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06978146200018 [Primary] |
| GS1 | 16978146200015 [Package] Contains: 06978146200018 Package: [32 Units] In Commercial Distribution |
| GS1 | 26978146200012 [Package] Contains: 06978146200018 Package: [36 Units] In Commercial Distribution |
| GS1 | 36978146200019 [Package] Contains: 06978146200018 Package: [48 Units] In Commercial Distribution |
| NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-17 |
| Device Publish Date | 2025-01-09 |
| 16978146200091 | TENS & PMS Unit |
| 16978146200084 | TENS & PMS Unit |
| 16978146200077 | TENS & PMS Unit |
| 16978146200060 | TENS & PMS Unit |
| 16978146200053 | TENS & PMS Unit |
| 16978146200046 | TENS & PMS Unit |
| 16978146200039 | TENS & PMS Unit |
| 16978146200022 | TENS & PMS Unit |
| 16978146200015 | TENS & PMS Unit |
| 16978146200008 | TENS & PMS Unit |
| 16978146200107 | TENS & PMS Unit |