In order to provide our customers with consistent quality, we work according to common standards. Thanks to our various certifications, we meet the different requirements of a wide range of industries. We are also member of several associations to better understand the individual requirements of our customers.
DIN EN ISO 9001
The process-oriented quality management system accompanies all essential operational processes and puts them under test. In this way, processes can be optimised and improved. This is to your benefit as a customer through our top-quality products.
Railway - ISO/TS 22163 (IRIS) and DIN EN 15085-2/CL4 (Welding)
IRIS certification (International Railway Industry Standard) for auxiliary systems scope. Development, production, sales and customer service of compressors, vacuum pumps, system solutions and end-user products in the railway industry. This certificate is a hallmark of the quality suppliers to the railway Industry.
Medicine certification - EN ISO 13485
Products to be used in medical-technical applications must meet high reliability and safety requirements. For this reason Dürr Technik is ISO 13485 certified. Our certificate applies to the development, manufacture, sales and customer service of compressors, vacuum pumps, specific system solutions and end-user products.
Medical device IIb according to 93/42/EWG
Medical devices must meet certain requirements in order to ensure patient safety and product quality. Directive 93/42/EEC on medical devices is the most important regulatory instrument for demonstrating the safety and medical performance of medical devices in the European Economic Area. Our product SICOLAB med has the necessary certification as a Class IIb medical device according to 93/42/EEC and is approved in the EU with the EC certificate, according to Article 120 of the European Medical Devices Regulation, (EU) 2017/745 (MDR).
Medical Device Class I according to the European Medical Device Regulation, (EU) 2017/745 (MDR).
Dürr Technik's SICOLAB mini ENDO has the necessary certification as a Class I medical system in accordance with Regulation (EU) 2017/745, making the product the first compressor station with stainless steel compressed air gun on the market to be approved for drying endoscopes and MIS instruments as a Class I medical system in accordance with the European Medical Device Regulation MDR 2017/745. When Regulation (EU) 2017/745 on medical devices (MDR) comes into force on May 26, 2020, Directives 90/385/EEC and 93/42/EEC will be replaced. Products which are certified according to Directive 93/42/EEC are subject to transitional regulations. For example, the SICOLAB med compressor for ventilators, as a legacy device, continues to be approved as a medical device under current law until the end of its device approval.
Explosion protection - ATEX-Certification
according to directive 2014/34/EU for the product line piston pumps approved by the Physikalisch-Technische Bundesanstalt Braunschweig and Berlin. The production of our MEX vapor recovery pumps, which are then installed in petrol dispensers, is monitored in accordance with ISO/IEC 80079-34 (Certified with the Recognition of Quality Assurance in Production - QAN). Our vapour recovery pumps MEX, which are fitted in petrol pumps, have this certificate besides an EG type examination certificate.
EAC Russian Federation (Formerly GOST) - Russian Quality Certification System for Imports
EAC is the Russian quality certification system which certifies. This certifies that our equipment complies with the standards applicable in Russia and CIS countries.
|ISO 9001_2015_until_2024_11_04_EN.pdf||(760.1 KiB)|
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