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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 6 of 60
DeviceModel / ReferenceRegistriesClassStatus
Demax DXQ100835N
FDA UDI
Class IIActive
Demax DQ07112121LT
FDA UDI
Class IIActive
Demax DXQ1108N18N
FDA UDI
Class IIActive
Demax DQ06233818S80
FDA UDI
Class IIActive
Demax DQ112338NTN
FDA UDI
Class IIActive
Demax DXQ072335N80
FDA UDI
Class IIActive
Demax DQ0523N21N
FDA UDI
Class IIActive
Demax DQ0808NNN
FDA UDI
Class IIActive
Demax DQ081521NTN
FDA UDI
Class IIActive
Demax DXQ0423N20LN
FDA UDI
Class IIActive
Demax DQ06232120LSN
FDA UDI
Class IIActive
Demax DQ041538NSN
FDA UDI
Class IIActive
Demax DXQ05083518
FDA UDI
Class IIActive
Demax DXQ04132120N
FDA UDI
Class IIActive
Demax DXQ08182520
FDA UDI
Class IIActive
Demax DXQ1011NNN
FDA UDI
Class IIActive
Demax DQ0418N20N
FDA UDI
Class IIActive
Demax DXQ071335N
FDA UDI
Class IIActive
Demax DQ0815N18
FDA UDI
Class IIActive
Demax DQ0911N18N
FDA UDI
Class IIActive
Demax DQ06083818S
FDA UDI
Class IIActive
Demax DQ1013N18N
FDA UDI
Class IIActive
Demax DXQ0815N20
FDA UDI
Class IIActive
Demax DHDT03B
FDA UDI
Class IIActive
Demax DXQ0515N18L
FDA UDI
Class IIActive
Demax DXQ04152520L
FDA UDI
Class IIActive
Demax DXQ0523252080
FDA UDI
Class IIActive
Demax DQ0618N20
FDA UDI
Class IIActive
Demax DXQ050825NN
FDA UDI
Class IIActive
Demax DXQ0513NNN
FDA UDI
Class IIActive
Demax DHD0914
FDA UDI
Class IIActive
Demax DXQ06232520LN
FDA UDI
Class IIActive
Demax DQ0518N20N
FDA UDI
Class IIActive
Demax DQ04152121S
FDA UDI
Class IIActive
Demax DQ07083818T
FDA UDI
Class IIActive
Demax DQ06113818SN
FDA UDI
Class IIActive
Demax DPY03B
FDA UDI
Class IIActive
Demax DXQ08152120LN
FDA UDI
Class IIActive
Demax DQ09233818S80
FDA UDI
Class IIActive
Demax DQ06232120S80
FDA UDI
Class IIActive
Demax DQ0813N18N
FDA UDI
Class IIActive
Demax DXQ09232520N80
FDA UDI
Class IIActive
Demax DQ08152120TN
FDA UDI
Class IIActive
Demax DQ040821NT
FDA UDI
Class IIActive
Demax DQ0823N18N
FDA UDI
Class IIActive
Demax DXQ0408NN
FDA UDI
Class IIActive
Demax DXQ0918N20N
FDA UDI
Class IIActive
Demax DXQ09132520N
FDA UDI
Class IIActive
Demax DQ0908N20
FDA UDI
Class IIActive
Demax DQ10133818SN
FDA UDI
Class IIActive

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