| Primary Device ID | 00860004687528 |
| NIH Device Record Key | f099e54e-80ee-41d4-b0fa-4f2a05d7a744 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pro Cellular Blood Pressure Monitor |
| Version Model Number | RPD-3250 |
| Company DUNS | 121900487 |
| Company Name | Remote Patient Devices LLC |
| 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 | true |
| 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 | 00860004687528 [Primary] |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-01-10 |
| Device Publish Date | 2021-12-31 |
| 00860004687535 - TeleRPM Blood Glucose Monitoring System | 2024-01-31 |
| 00860004687542 - TeleRPM Blood Glucose Meter | 2024-01-31 |
| 00860004687559 - TeleRPM Blood Glucose Test Strip | 2024-01-31 |
| 00860004687566 - Control Solution | 2024-01-31 |
| 00860004687573 - Single Use Lancets | 2024-01-31 |
| 00860004687580 - Lancing Device | 2024-01-31 |
| 00860004687528 - Pro Cellular Blood Pressure Monitor | 2022-01-10 |
| 00860004687528 - Pro Cellular Blood Pressure Monitor | 2022-01-10 |