H-E-B inControl

FDA UDI

Class II (US FDA UDI)

by Shenzhen Jumper Medical Equipment Co., Ltd.

Identity

Trade Name: H-E-B inControl FDA UDI
Generic Name: Infrared patient thermometer, ear/skin FDA UDI
Model / Reference: JPD-FR403 FDA UDI

Identifiers

Primary DI / UDI-DI: 06951740500654 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Infrared patient thermometer, ear/skin

H-E-B inControl 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.

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FIGHTECH — Shenzhen Urion Technology Co., Ltd. · Class II
Infrared Thermometer — Shenzhen Pacom Medical Instruments Co., Ltd. · Class II
MOBI — MOBI TECHNOLOGIES, INC. · Class II
CONAIR CORPORATION — CONAIR LLC. · Class II
AlphaMed — Shenzhen Urion Technology Co., Ltd. · Class II
Caroune — Shenzhen Pacom Medical Instruments Co., Ltd. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Shenzhen Jumper Medical Equipment Co., Ltd.

Sources (1)

FDA UDI a3782ecf-2d00-4b51-8eda-a9ce3bb87839 32 fields · synced May 29, 2026