| Primary Device ID | 10810140060454 |
| NIH Device Record Key | 8e7e4526-6a6d-49e2-9520-596adcfb1d23 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RENPHO Smart Eye Massager |
| Version Model Number | RF-EM001S |
| Company DUNS | 033774836 |
| Company Name | Joicom Corporation |
| 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 | 00810140060457 [Primary] |
| GS1 | 10810140060454 [Package] Contains: 00810140060457 Package: case [16 Units] In Commercial Distribution |
| GS1 | 20810140060451 [Package] Contains: 00810140060457 Package: case [16 Units] In Commercial Distribution |
| ISA | Massager, Therapeutic, Electric |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-15 |
| Device Publish Date | 2023-08-07 |
| 10810140062892 - RENPHO | 2026-01-12 |
| 10810140062908 - RENPHO | 2026-01-12 |
| 10810140062861 - RENPHO | 2025-12-24 Foot Massager |
| 10810140062854 - RENPHO | 2025-12-11 Massage Gun |
| 10810140062847 - RENPHO | 2025-12-03 |
| 10810140062670 - RENPHO | 2025-09-19 Massage Gun |
| 10810140062298 - iDOO Heating Pad | 2025-09-08 |
| 10810140062656 - PureHeal | 2025-08-28 Foot massager |