| Primary Device ID | 10810140060744 |
| NIH Device Record Key | addc31c0-f544-47fd-aa8e-daa6cf1b041f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RENPHO Smart scale |
| Version Model Number | R-A020 |
| 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 | 00810140060747 [Primary] |
| GS1 | 10810140060744 [Package] Contains: 00810140060747 Package: case [5 Units] In Commercial Distribution |
| PUH | Analyzer, Body Composition, Exempt |
| 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 |
| 10810140060744 | R-A020 |
| 10810140060737 | R-A020 |
| 10810140060720 | R-A011 |
| 10810140060690 | R-A016 |
| 10810140060669 | R-A016 |
| 10810140060652 | R-A001 |
| 10810140060638 | R-A005 |
| 10810140060621 | ES-BR001 |
| 10810140060553 | R-A002 |
| 10810140060096 | ES-WBE28 |
| 10810140060072 | R-A012 |