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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 5 of 60
DeviceModel / ReferenceRegistriesClassStatus
Demax DQ0808N18
FDA UDI
Class IIActive
Demax DXQ11233518LN
FDA UDI
Class IIActive
Demax DQ061821NTN
FDA UDI
Class IIActive
Demax DHDY01B
FDA UDI
Class IIActive
Demax DQ04112120LTN
FDA UDI
Class IIActive
Demax DQ0523NNN
FDA UDI
Class IIActive
Demax DQ051821NTN
FDA UDI
Class IIActive
Demax DQ0513N18N
FDA UDI
Class IIActive
Demax DQ110838NT
FDA UDI
Class IIActive
Demax DXQ04112520LN
FDA UDI
Class IIActive
Demax DBQ06162120S80
FDA UDI
Class IIActive
Demax DQ07132120LS
FDA UDI
Class IIActive
Demax DXQ0723252080
FDA UDI
Class IIActive
Demax DXQ0623N20L
FDA UDI
Class IIActive
Demax DXQ0623N18
FDA UDI
Class IIActive
Demax DXQ041835N
FDA UDI
Class IIActive
Demax DXQ0808N20N
FDA UDI
Class IIActive
Demax DQ081521NSN
FDA UDI
Class IIActive
Demax DQ06112120LTN
FDA UDI
Class IIActive
Demax DQ05152120S
FDA UDI
Class IIActive
Demax DQ05112120TN
FDA UDI
Class IIActive
Demax DXQ04132520N
FDA UDI
Class IIActive
Demax DXQ09132520
FDA UDI
Class IIActive
Demax DQ06112120SN
FDA UDI
Class IIActive
Demax DXQ0408N20N
FDA UDI
Class IIActive
Demax DQ06113818T
FDA UDI
Class IIActive
Demax DXQ1013NN
FDA UDI
Class IIActive
Demax DXQ081835NN
FDA UDI
Class IIActive
Demax DHDY03B
FDA UDI
Class IIActive
Demax DXQ081521N
FDA UDI
Class IIActive
Demax DXQ091135NN
FDA UDI
Class IIActive
Demax DQ06182120SN
FDA UDI
Class IIActive
Demax DQ0408N20L
FDA UDI
Class IIActive
Demax DQ072321NSN80
FDA UDI
Class IIActive
Demax DXQ081525N
FDA UDI
Class IIActive
Demax DQ0708N21
FDA UDI
Class IIActive
Demax DXQ0418N20
FDA UDI
Class IIActive
Demax DXQ1023NN
FDA UDI
Class IIActive
Demax DXQ07132520L
FDA UDI
Class IIActive
Demax DQ0918N21N
FDA UDI
Class IIActive
Demax DQ07232120LSN80
FDA UDI
Class IIActive
Demax DQ040838NSN
FDA UDI
Class IIActive
Demax DXQ0808N18LN
FDA UDI
Class IIActive
Demax DQ0415N20L
FDA UDI
Class IIActive
Demax DXQ04113518N
FDA UDI
Class IIActive
Demax DXQ041521N
FDA UDI
Class IIActive
Demax DXQ0408N20LN
FDA UDI
Class IIActive
Demax DXQ0413N20N
FDA UDI
Class IIActive
Demax DXQ08153518
FDA UDI
Class IIActive
Demax DQ04183818TN
FDA UDI
Class IIActive

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