| Primary Device ID | 00810140062154 |
| NIH Device Record Key | dfb802a3-f6fc-41cb-9ff1-970af7452939 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RENPHO Heating Pad |
| Version Model Number | R-HAP02 |
| 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 | 00810140062154 [Primary] |
| GS1 | 10810140062151 [Package] Package: case [8 Units] In Commercial Distribution |
| IRT | Pad, Heating, Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-06 |
| Device Publish Date | 2025-05-29 |
| 10810140061161 | R-U011 |
| 10810140061130 | NA-H1222D |
| 10810140061123 | NA-H1222D |
| 10810140061116 | NA-H1222D |
| 10810140061109 | NA-H1222D |
| 10810140061093 | NA-H1222D |
| 10810140061086 | NA-H1222D |
| 10810140061079 | R-U002 |
| 10810140061062 | R-U002 |
| 10810140061055 | R-U002 |
| 10810140061048 | R-U005 |
| 10810140061031 | R-U006 |
| 10810140061024 | R-U006 |
| 10810140061017 | R-U006 |
| 10810140061000 | R-U010 |
| 00810140062260 | R-HAP68 |
| 00810140062253 | R-HAP67 |
| 00810140062246 | R-HAP64 |
| 00810140062178 | R-HAP61 |
| 00810140062161 | R-HAP03 |
| 00810140062154 | R-HAP02 |
| 00810140062147 | R-HAP01 |