Supplier information - Statistics Business concept

Supplier information


Supplier information

On this page you will find everything you need to know about how Dräger works with its suppliers. Please get in touch with your Purchasing contact if you have any questions.

General purchasing information

All orders are exclusively subject to Dräger’s currently valid General Terms and Conditions of Purchase, which are attached below. Any delivery conditions deviating from these terms only apply if they have been expressly accepted by us in writing.

Supply Chain Handbook for Suppliers

This handbook sets a framework for our Supply Chain partnership and combines our understanding of Supply Chain Management with our approach to collaboration.

Business people negotiating a contract

REACh and RoHs regulations

Dräger products protect, support and save lives. As a result, it is essential to meet both technical and environmental requirements worldwide. These environmental requirements often include restrictions or declaration requirements for certain substances that are defined in guidelines such as the REACh Regulation (EC) No. 1907/2006, the RoHS Directive 2011/65/EU (and RoHSII) and the Medical Devices Regulation 2017/745 (MDR), which entered into force in 2020.

It is crucial for Dräger to look beyond the currently applicable requirements and obtain further information about substances in products and their components. The Dräger Substance Radar initiative fulfils this aim.

On the following pages, you can find information about the Dräger Substance Radar, the REACH Regulation, the RoHSII Directive and the Medical Devices Regulation. We also provide further explanations about how to proceed as a supplier.

REACh and RoHs regulations

Scientist with laboratory background

Dräger Substance Radar (incl. REACh)

Dräger Substance Radar (DSR) is an initiative for the early detection of potentially harmful substances.

Dräger Substance Radar (incl. REACh)

Electronic Industry


For Dräger as a manufacturer, all products that we bring to market must be RoHS compliant. This means that all components and structural elements that are part of Dräger products must also comply with this regulation.


Babyleo Neonatal Showroom

Medical Device Regulation (MDR)

Medical devices and product components, as well as the materials contained in medical devices, are subject to special declaration obligations. Suppliers preferably provide information with regard to parts that potentially contain materials and substances affected by the regulation. Dräger will let you know if this applies to your products as part of the purchasing process.




On 6th January 2021, the United States Environmental Protection Agency (US. EPA) announced a ban on the manufacture, use and distribution in commerce of 5 Persistent, Bioaccumulative and Toxic (PBT) substances including articles containing these substances. For details see under 40 CFR Part 751, Subpart E. The new rules went into effect on 8th March 2021 for four of the substances except for PIP 3:1, which has its implementation deadline extended to October 31st, 2024. For Dräger as a manufacturer, all products that we bring to market in the USA must be TSCA compliant. This means that all components and elements that are part of Dräger products must also comply with this regulation.

Substance ban under TSCA Section 6 (h)

Growing Tree / Love Nature

Code of Conduct for Business Partners

Our Code of Conduct for Business Partners contains the basic requirements for all our business partners and suppliers. Click on the following link for more details.

Code of Conduct for Business Partners

Contact Dräger


Drägerwerk AG & Co. KGaA

Moislinger Allee 53–55

23558 Lübeck

+49 451 882 0

There for you 24/7.