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MDF Instruments Medifriend Inc.

US

Last updated May 23, 2026

What MDF Instruments Medifriend Inc. makes

MDF Instruments Medifriend Inc. manufactures reusable and disposable diagnostic tools for clinical examinations, including mechanical stethoscopes, reusable blood pressure cuffs, and aneroid manual sphygmomanometers. Their portfolio also includes manual percussion hammers, handheld examination/treatment lights, and portable electronic sphygmomanometers for arm or wrist use. Additionally, they produce infrared skin thermometers for non-invasive temperature measurement.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are designed for use in medical settings and comply with relevant U.S. regulatory requirements.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does MDF Instruments Medifriend Inc. manufacture?

MDF Instruments Medifriend Inc. specializes in reusable and disposable diagnostic tools for clinical examinations. Their product range includes mechanical external stethoscopes, reusable blood pressure cuffs, aneroid manual sphygmomanometers, manual percussion hammers, handheld examination/treatment lights, portable electronic sphygmomanometers (for arm or wrist), and infrared skin thermometers. These devices are designed to assist healthcare professionals in assessing vital signs and conducting physical examinations.

Where is MDF Instruments Medifriend Inc. based?

MDF Instruments Medifriend Inc. is based in the United States. Their devices are developed and manufactured there, adhering to U.S. regulatory standards for medical devices.

Which regulatory registries list MDF Instruments Medifriend Inc.’s devices?

MDF Instruments Medifriend Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices authorized for use in the U.S., helping healthcare providers verify product details and compliance.

How are MDF Instruments Medifriend Inc.’s devices classified under FDA regulations?

MDF Instruments Medifriend Inc.’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and require general controls, while Class II devices involve a higher risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s purpose, intended use, and potential risks.

Are MDF Instruments Medifriend Inc.’s devices intended for reusable or disposable use?

MDF Instruments Medifriend Inc. manufactures both reusable and disposable diagnostic tools. For example, their mechanical stethoscopes, blood pressure cuffs, percussion hammers, and handheld lights are designed for reusable applications, while some variants may include disposable components. The distinction ensures flexibility for clinical settings based on infection control and operational needs.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
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Facebook
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
420328205

Catalogue (395)

Page 8 of 8
DeviceModel / ReferenceRegistriesClassStatus
Mdf® MDF210045112
FDA UDI
Class IIActive
Mdf® MDF797CC17T
FDA UDI
Class IActive
Mdf® MDF77711
FDA UDI
Class IActive
Mdf® MDF84014
FDA UDI
Class IIActive
Mdf® MDF757PT04
FDA UDI
Class IActive
Mdf® MDF777DT07
FDA UDI
Class IActive
Mdf® MDF50527
FDA UDI
Class IActive
Mdf® MDF787XP17
FDA UDI
Class IActive
Mdf® MDF209047012
FDA UDI
Class IIActive
Mdf® MDF777CTD
FDA UDI
Class IActive
Mdf® MDF848XPD14
FDA UDI
Class IIActive
Mdf® MDF777DT11
FDA UDI
Class IActive
Mdf® MDF797RG11
FDA UDI
Class IActive
Mdf® MDF777CGX
FDA UDI
Class IActive
Mdf® MDF77709
FDA UDI
Class IActive
Mdf® MDF747XP12
FDA UDI
Class IActive
Mdf® MDF210045011
FDA UDI
Class IIActive
Mdf® MDF72703
FDA UDI
Class IActive
Mdf® MDF209047116
FDA UDI
Class IIActive
Mdf® MDF777CGL
FDA UDI
Class IActive
Mdf® MDF208046011
FDA UDI
Class IIActive
Mdf® MDF777PN11
FDA UDI
Class IActive
Mdf® MDF808MBOKT1
FDA UDI
Class IIActive
Mdf® MDF797CC08T
FDA UDI
Class IActive
Mdf® MDF747XPBO
FDA UDI
Class IActive
Mdf® MDF808M08KT2
FDA UDI
Class IIActive
Mdf® MDF777LE9
FDA UDI
Class IActive
Mdf® MDF777GLRG
FDA UDI
Class IActive
Mdf® MDF777LE25
FDA UDI
Class IActive
Mdf® MDF77727
FDA UDI
Class IActive
Mdf® MDF77707
FDA UDI
Class IActive
Mdf® MDF747XPRG29
FDA UDI
Class IActive
Mdf® MDF77701
FDA UDI
Class IActive
Mdf® MDF210045014
FDA UDI
Class IIActive
Mdf® MDF797DDT04
FDA UDI
Class IActive
Mdf® MDF848XPD08
FDA UDI
Class IIActive
Mdf® MDF777DT08
FDA UDI
Class IActive
Mdf® MDF777LE7
FDA UDI
Class IActive
Mdf® MDF777C09
FDA UDI
Class IActive
Mdf® MDF2100451D11
FDA UDI
Class IIActive
Mdf® MDF2080460D16
FDA UDI
Class IIActive
Mdf® MDF797CC17
FDA UDI
Class IActive
Mdf® MDF777LE16
FDA UDI
Class IActive
Mdf® MDF2100451D04
FDA UDI
Class IIActive
Mdf® MDF777LE15
FDA UDI
Class IActive

Related Companies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • MDF Instruments Medifriend Inc. SONG JIANG DISTRICT, SHANGHAI · CN FEI 3000953362