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AlphaMed

FDA UDI

Class II (US FDA UDI)

by Shenzhen Urion Technology Co., Ltd.

Identity

Trade Name
AlphaMed FDA UDI
Generic Name
Infrared patient thermometer, ear/skin FDA UDI
Model / Reference
UFR109 FDA UDI

Identifiers

Primary DI / UDI-DI
06953825904036 FDA UDI
510(k) Number
K200802 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, ear/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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Infrared patient thermometer, ear/skin

AlphaMed by Shenzhen Urion Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, ear/skin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6be4334c-665a-43d5-90b2-b34b19f4b458 33 fields · synced May 30, 2026