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Bestmed

FDA UDI

Class II (US FDA UDI)

by 180 Innovations Llc

Identity

Trade Name
Bestmed FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
A hand-held battery powered, electronic instrument designed to measure a patient's body temperature from the forehead. The device has a rigid tip and a LCD display. It is designed to take a temperature reading. This is a reusable device. FDA UDI
Model / Reference
HTD8813C FDA UDI
Description
A hand-held battery powered, electronic instrument designed to measure a patient's body temperature from the forehead. The device has a rigid tip and a LCD display. It is designed to take a temperature reading. This is a reusable device. FDA UDI

Identifiers

Primary DI / UDI-DI
00809148200750 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Intermittent electronic patient thermometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intermittent electronic patient thermometer

Bestmed by 180 Innovations Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent electronic patient thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
180 Innovations Llc

Sources (1)

  • FDA UDI 96f1f6b4-ef6f-4168-9577-1c77b9ea4f73 33 fields · synced May 30, 2026