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femometer family

FDA UDI

Class II (US FDA UDI)

by Hetaida Technology Co., Ltd

Identity

Trade Name
femometer family FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Device Name
Infrared Body Thermometer FDA UDI
Model / Reference
K8832US FDA UDI
Description
Infrared Body Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
06970289035625 FDA UDI
510(k) Number
K200159 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, skin 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

Yes

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: Infrared patient thermometer, skin

femometer family by Hetaida Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, skin.

Cleared under the same submission

K200159 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b2df3a04-3ba1-4019-b87f-9129fe1f078b 36 fields · synced Jun 8, 2026