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Beijing Demax Medical Technology Co., Ltd

US

Last updated May 23, 2026

What Beijing Demax Medical Technology Co., Ltd makes

The company manufactures single-use and reusable medical devices for vascular procedures, including catheter introduction sets, haemostasis valves, and pneumatic tourniquet systems. It also produces arm positioners for procedural support and catheter/overtube balloon inflators. These products are designed for use in clinical settings requiring precise vascular access and controlled haemostasis.

The portfolio includes devices classified as Class I and Class II under regulatory frameworks, with listings in the FDA’s Unique Device Identifier (UDI) database. The company operates with a US presence, adhering to applicable medical device regulations.

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 Beijing Demax Medical Technology Co., Ltd manufacture?

Beijing Demax Medical Technology Co., Ltd specializes in vascular procedure devices, including single-use and reusable products. Their portfolio covers catheter introduction sets (nonimplantable), haemostasis valves, rotating pneumatic tourniquet systems, arm procedure positioners (reusable), and catheter/overtube balloon inflators. These devices are designed to support precise vascular access, haemostasis control, and procedural stability in clinical environments.

Where is Beijing Demax Medical Technology Co., Ltd based, and how does this affect its regulatory compliance?

The company has a presence in the United States, which means its devices must comply with FDA regulations. Since the US is a key market, their products are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and regulatory transparency for healthcare providers and authorities.

Which regulatory classifications apply to Beijing Demax Medical Technology Co., Ltd’s devices?

Beijing Demax’s devices fall under Class I and Class II regulatory classifications. Class I devices generally pose minimal risk and may require less stringent premarket review, while Class II devices involve moderate risk and typically require special controls or performance standards to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential health impact.

Are Beijing Demax Medical Technology Co., Ltd’s devices listed in any regulatory registries?

Yes, the company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps healthcare providers, regulators, and supply chain partners track and verify device information, ensuring proper identification and compliance with US medical device regulations.

How are Beijing Demax Medical Technology Co., Ltd’s devices categorized in terms of reuse?

The company manufactures both single-use and reusable devices. Single-use items like catheter introduction sets and balloon inflators are designed for one-time use to minimize infection risk, while reusable products—such as arm procedure positioners and some tourniquet systems—are engineered for sterilization and repeated clinical use, adhering to strict cleaning and reprocessing protocols.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
529725666

Catalogue (2953)

Page 7 of 60
DeviceModel / ReferenceRegistriesClassStatus
Demax DQ1123NN
FDA UDI
Class IIActive
Demax DQ091138NSN
FDA UDI
Class IIActive
Demax DQ04233818T80
FDA UDI
Class IIActive
Demax DMK-T-02(OFF)
FDA UDI
Class IIActive
Demax DQ0908N18N
FDA UDI
Class IIActive
Demax DXQ0515N18
FDA UDI
Class IIActive
Demax DQ072338NTN80
FDA UDI
Class IIActive
Demax DQ07132120TN
FDA UDI
Class IIActive
Demax DQ0518N20LN
FDA UDI
Class IIActive
Demax DXQ05152520LN
FDA UDI
Class IIActive
Demax DXQ07232120L80
FDA UDI
Class IIActive
Demax DQ09152120LTN
FDA UDI
Class IIActive
Demax DQ0423NN
FDA UDI
Class IIActive
Demax DXQ0615N20
FDA UDI
Class IIActive
Demax DBQ05102120T
FDA UDI
Class IIActive
Demax DQ0411NNN
FDA UDI
Class IIActive
Demax DXQ0913N20LN
FDA UDI
Class IIActive
Demax DQ101138NSN
FDA UDI
Class IIActive
Demax DHRY01B
FDA UDI
Class IIActive
Demax DXQ0908N20N
FDA UDI
Class IIActive
Demax DXQ081135NN
FDA UDI
Class IIActive
Demax DXQ04082120LN
FDA UDI
Class IIActive
Demax DQ0418NNN
FDA UDI
Class IIActive
Demax DXQ04112120N
FDA UDI
Class IIActive
Demax DQ04083818T
FDA UDI
Class IIActive
Demax DXQ04113518L
FDA UDI
Class IIActive
Demax DXQ07112120
FDA UDI
Class IIActive
Demax DQ081338NS
FDA UDI
Class IIActive
Demax DQ0413N18
FDA UDI
Class IIActive
Demax DXQ08182120N
FDA UDI
Class IIActive
Demax DQ0615NN
FDA UDI
Class IIActive
Demax DXQ04132120LN
FDA UDI
Class IIActive
Demax DXQ04083518L
FDA UDI
Class IIActive
Demax DQ05083818TN
FDA UDI
Class IIActive
Demax DQ05152120SN
FDA UDI
Class IIActive
Demax DXQ0915N20
FDA UDI
Class IIActive
Demax DQ1108N18
FDA UDI
Class IIActive
Demax DQ0508NN
FDA UDI
Class IIActive
Demax DQ1008N18N
FDA UDI
Class IIActive
Demax DQ09082121T
FDA UDI
Class IIActive
Demax DXQ1118N18L
FDA UDI
Class IIActive
Demax DXQ0913N18
FDA UDI
Class IIActive
Demax DQ08233818T80
FDA UDI
Class IIActive
Demax DQ07182120LTN
FDA UDI
Class IIActive
Demax DHD0922
FDA UDI
Class IIActive
Demax DXQ09083518L
FDA UDI
Class IIActive
Demax DXQ05112520L
FDA UDI
Class IIActive
Demax DXQ071835N
FDA UDI
Class IIActive
Demax DXQ0523NNN
FDA UDI
Class IIActive
Demax DQ061821NSN
FDA UDI
Class IIActive

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