| Primary Device ID | 00860002249667 |
| NIH Device Record Key | 3ce1e26a-6907-4ac7-a14d-f2e158d4dd61 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RENPHO Infrared Forehead Thermometer |
| Version Model Number | DET-306 |
| Company DUNS | 081060692 |
| 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 | true |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860002249667 [Primary] |
| GS1 | 30860002249668 [Package] Package: Carton [100 Units] In Commercial Distribution |
| FLL | Thermometer, Electronic, Clinical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-31 |
| Device Publish Date | 2020-07-23 |
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