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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 4 of 60
DeviceModel / ReferenceRegistriesClassStatus
Demax DXQ0415N18L
FDA UDI
Class IIActive
Demax DQ06232121TN
FDA UDI
Class IIActive
Demax DQ0613NNN
FDA UDI
Class IIActive
Demax DQ0523N20LN
FDA UDI
Class IIActive
Demax DXQ08132520LN
FDA UDI
Class IIActive
Demax DQ08233818TN
FDA UDI
Class IIActive
Demax DXQ1115N18LN
FDA UDI
Class IIActive
Demax DXQ09232520N
FDA UDI
Class IIActive
Demax DXQ09112120LN
FDA UDI
Class IIActive
Demax DXQ1111N18
FDA UDI
Class IIActive
Demax DXQ082335N80
FDA UDI
Class IIActive
Demax DXQ06112520
FDA UDI
Class IIActive
Demax DQ05082120LT
FDA UDI
Class IIActive
Demax DXQ1018N18
FDA UDI
Class IIActive
Demax DXQ0908N18L
FDA UDI
Class IIActive
Demax DXQ08183518
FDA UDI
Class IIActive
Demax DXQ0713N20N
FDA UDI
Class IIActive
Demax DXQ09232120L80
FDA UDI
Class IIActive
Demax DXQ05232120L
FDA UDI
Class IIActive
Demax DXQ091335N
FDA UDI
Class IIActive
Demax DQ04132120LTN
FDA UDI
Class IIActive
Demax DXQ08083518L
FDA UDI
Class IIActive
Demax DQ09082120TN
FDA UDI
Class IIActive
Demax DXQ082325N80
FDA UDI
Class IIActive
Demax DQ112338NS80
FDA UDI
Class IIActive
Demax DXQ0923N20
FDA UDI
Class IIActive
Demax DQ0423NNN
FDA UDI
Class IIActive
Demax DQ100838NS
FDA UDI
Class IIActive
Demax DXQ081121NN
FDA UDI
Class IIActive
Demax DXQ112335NN
FDA UDI
Class IIActive
Demax DQ0923N20LN
FDA UDI
Class IIActive
Demax DQ09152121S
FDA UDI
Class IIActive
Demax DXQ092321N80
FDA UDI
Class IIActive
Demax DQ112338NT80
FDA UDI
Class IIActive
Demax DBT04L
FDA UDI
Class IActive
Demax DQ0923N18
FDA UDI
Class IIActive
Demax DXQ071321N
FDA UDI
Class IIActive
Demax DQ052321NTN
FDA UDI
Class IIActive
Demax DQ0711N20LN
FDA UDI
Class IIActive
Demax DXQ0613N20N
FDA UDI
Class IIActive
Demax DQ071838NTN
FDA UDI
Class IIActive
Demax DXQ06232120L
FDA UDI
Class IIActive
Demax DQ062321NT80
FDA UDI
Class IIActive
Demax DXQ080825N
FDA UDI
Class IIActive
Demax DXQ0615N20L
FDA UDI
Class IIActive
Demax DXQ0618NNN
FDA UDI
Class IIActive
Demax DQ082338NS80
FDA UDI
Class IIActive
Demax DQ051121NT
FDA UDI
Class IIActive
Demax DXQ0613N18L
FDA UDI
Class IIActive
Demax DXQ05112120N
FDA UDI
Class IIActive

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