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Infrared Thermometer

FDA UDI

Class II (US FDA UDI)

by Shenzhen Jumper Medical Equipment Co., Ltd.

Identity

Trade Name
Infrared Thermometer FDA UDI
Generic Name
Infrared patient thermometer, ear/skin FDA UDI
Model / Reference
JPD-FR408 FDA UDI

Identifiers

Primary DI / UDI-DI
06951740501255 FDA UDI
510(k) Number
K131243 FDA UDI
K172795 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Infrared patient thermometer, ear/skin

Infrared Thermometer by Shenzhen Jumper Medical Equipment 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 a0f54afe-8e0d-4ab5-b8f0-67c3a9d8cb0b 33 fields · synced May 30, 2026