Supplier information - Statistics Business concept

Supplier information

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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.

Law Book

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.

Download General Terms and Conditions of Purchase

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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

RoHS

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.

RoHS

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.

MDR

Growing Tree / Love Nature

Supplier principles

Our supplier principles contain the basic requirements for all our business partners and suppliers. Click on the following link for more details.

Supplier principles

Contact Dräger

Envelope

Drägerwerk AG & Co. KGaA

Moislinger Allee 53–55

23558 Lübeck

+49 451 882 0

There for you 24/7.