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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 3 of 60
DeviceModel / ReferenceRegistriesClassStatus
Demax DXQ0711NN
FDA UDI
Class IIActive
Demax DQ07232120S80
FDA UDI
Class IIActive
Demax DQ07232120LTN80
FDA UDI
Class IIActive
Demax DQ07233818SN80
FDA UDI
Class IIActive
Demax DQ0513N18
FDA UDI
Class IIActive
Demax DQ09083818SN
FDA UDI
Class IIActive
Demax DXQ05133518L
FDA UDI
Class IIActive
Demax DQ0913N18N
FDA UDI
Class IIActive
Demax DQ082321NTN
FDA UDI
Class IIActive
Demax DQ0513NN
FDA UDI
Class IIActive
Demax DXQ0811N18N
FDA UDI
Class IIActive
Demax DXQ0923N20L
FDA UDI
Class IIActive
Demax DXQ09152120N
FDA UDI
Class IIActive
Demax DQ092321NT80
FDA UDI
Class IIActive
Demax DXQ05112120L
FDA UDI
Class IIActive
Demax DXQ0811NN
FDA UDI
Class IIActive
Demax DXQ0423N20L
FDA UDI
Class IIActive
Demax DQ05232120TN
FDA UDI
Class IIActive
Demax DQ0523NN
FDA UDI
Class IIActive
Demax DQ0415N21
FDA UDI
Class IIActive
Demax DXQ07182120L
FDA UDI
Class IIActive
Demax DXQ09082520
FDA UDI
Class IIActive
Demax DHDT01B
FDA UDI
Class IIActive
Demax DQ05233818S80
FDA UDI
Class IIActive
Demax DXQ09182520L
FDA UDI
Class IIActive
Demax DXQ0423252080
FDA UDI
Class IIActive
Demax DXQ092321NN80
FDA UDI
Class IIActive
Demax DQ0815N21N
FDA UDI
Class IIActive
Demax DXQ0808N18
FDA UDI
Class IIActive
Demax DXQ08112120N
FDA UDI
Class IIActive
Demax DXQ0613NNN
FDA UDI
Class IIActive
Demax DQ07182121TN
FDA UDI
Class IIActive
Demax DQ07112120T
FDA UDI
Class IIActive
Demax DXQ04183518LN
FDA UDI
Class IIActive
Demax DQ06182120LSN
FDA UDI
Class IIActive
Demax DQ06232121LT80
FDA UDI
Class IIActive
Demax DQ081538NSN
FDA UDI
Class IIActive
Demax DXQ04152120LN
FDA UDI
Class IIActive
Demax DQ10233818TN80
FDA UDI
Class IIActive
Demax DXQ08182520N
FDA UDI
Class IIActive
Demax DQ06112120LT
FDA UDI
Class IIActive
Demax DQ0815N21
FDA UDI
Class IIActive
Demax DQ06153818T
FDA UDI
Class IIActive
Demax DXQ0723NNN
FDA UDI
Class IIActive
Demax DQ08112121SN
FDA UDI
Class IIActive
Demax DXQ0818N20LN
FDA UDI
Class IIActive
Demax DQ072321NT80
FDA UDI
Class IIActive
Demax DQ05112120LT
FDA UDI
Class IIActive
Demax DXQ04112520
FDA UDI
Class IIActive
Demax DQ0418N18
FDA UDI
Class IIActive

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