| Primary Device ID | 10810140060423 |
| NIH Device Record Key | e210b2f1-48e4-4687-a6bf-aaa2c48ddf9d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RENPHO Eye Massager |
| Version Model Number | RF-EM001R |
| 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 | 00810140060426 [Primary] |
| GS1 | 10810140060423 [Package] Contains: 00810140060426 Package: case [12 Units] In Commercial Distribution |
| GS1 | 20810140060420 [Package] Contains: 00810140060426 Package: case [12 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 |
| 10810140060423 | RF-EM001R |
| 10810140060416 | RF-EM001R |
| 10810140060409 | RF-EM001 |
| 10810140060362 | RF-EM001 |
| 10810140060355 | RF-EM001 |