iHealth No-Touch Forehead Thermometer, Digital Infrared Thermometer for Adults and Kids, Touchless Baby Thermometer with 3 Ultra-Sensitive Sensors, Large LED Display and Gentle Vibration Alert (PT3)
$53.98
| Brand | IHealth |
| Power Source | Battery Powered |
| Number of Batteries | 2 AAA batteries required. (included) |
| Response Time | 1 seconds |
About this item
- No Touch Measuring, Just Safe and Hygienic: PT3 Built-in infrared temperature sensor, reads body temperature within 1.18 inches of the center of the forehead without physical contact.
- Tri-Point Sensors Accuracy: An ultra-sensitive infrared sensor collects more than 100 data points per second while distance and environmental sensors combine to account for other variables; ensuring maximum accuracy every time temperature is taken.
- Fast, Simple, Clear and Quiet: The intuitive single-button control design thermometer reads the temperature in just 1 second from a clear bright extra-large LED screen, even in total darkness. The quiet vibration alerting ensures there is no buzzing noise and no disturbance.
- Suitable for Multi-Scenario and All Ages: iHealth PT3 is designed for all ages: ranging from babies and toddlers to the elderly. An ideal choice for hospitals, hotels, school settings, and public establishments.
- What You Get: 1x PT3 thermometer, 2x AAA batteries, 1x Instruction manual, 1x Quick User Guide, our worry-free 12-month warranty, and friendly California-based customer service.
Important information
Legal Disclaimer
Statements regarding dietary supplements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease or health condition.
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- FDA Cleared is not the same as FDA Approved. Just because the device is "Cleared" does not mean it has been "Approved." Buyer beware - below is the terminology and it is not meant to be interchangeable:Clearance: When a medical device is cleared, this means it has undergone a 510(k) submission, which FDA has reviewed and provided clearance.Approval: For Class III medical devices to be legally marketed they must undergo a rigorous review and approval process. Following a successful submission of a premarket approval (PMA) or a Humanitarian Device Exemption (HDE), the device is given Approval by FDA. Granted: Medical devices using the De Novo pathway must be Granted by FDA before they can be legally marketed in the United States. This is a relatively new term in the FDA lexicon.answered on 2020-07-30 00:00:00
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