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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