| Primary Device ID | 10810140060997 |
| NIH Device Record Key | 717c77c6-bed4-414b-890f-a39335b3c04f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RENPHO Automatic Blood Pressure Monitor |
| Version Model Number | R-J004 |
| Company DUNS | 033774836 |
| Company Name | Joicom Corporation |
| 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 | 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 | 00810140060990 [Primary] |
| GS1 | 10810140060997 [Package] Contains: 00810140060990 Package: case [12 Units] In Commercial Distribution |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2025-02-17 |
| Device Publish Date | 2023-08-08 |
| 10810140060973 - RENPHO Blood Pressure Monitor | 2025-02-17 |
| 10810140060980 - RENPHO Blood Pressure Monitor | 2025-02-17 |
| 10810140060997 - RENPHO Automatic Blood Pressure Monitor | 2025-02-17 |
| 10810140060997 - RENPHO Automatic Blood Pressure Monitor | 2025-02-17 |
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| 20810140061359 - RENPHO | 2024-12-05 Foot massager |
| 00810140061218 - RENPHO | 2024-11-27 Massage Gun |
| 00810140061225 - RENPHO | 2024-11-27 Massage Gun |
| 00810140061270 - RENPHO | 2024-11-27 Foot Massager |