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Andnesfit Health

FDA UDI

Class II (US FDA UDI)

by Andesfit Limited

Identity

Trade Name
Andnesfit Health FDA UDI
Generic Name
Infrared patient thermometer, ear FDA UDI
Device Name
Wireless Infrared Ear/Forehead Thermometer FDA UDI
Model / Reference
ADF-34A FDA UDI
Description
Wireless Infrared Ear/Forehead Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
04897100310117 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, ear 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

Yes

FDA UDI

Category: Infrared patient thermometer, ear

Andnesfit Health by Andesfit Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, ear.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Andesfit Limited

Sources (1)

  • FDA UDI f85e6cd9-005f-4c71-bd51-a1cf32c5211e 33 fields · synced May 30, 2026