The Medical Devices Regulation (MDR) supersedes Directives 93/42/EEC and 90/385/EC, and this new law adopted by the European Parliament must be followed by medical devices manufacturers. The audits will be carried out by the “notified bodies”, the inspection agencies that review and assess the technical documentation for medical technology and have the legal power to shut down a company if the relevant requirements are not attended. The period to submit the audit required by the regulation is three years, up to May 2020. If we assume that the notified bodies can carry out the audits in about one year, thus the manufacturers will have only about two years to implement the MDR. Be prepared! This is an extremely tight time schedule. Click here to learn how to meet the requirements and save money!
Contact us for industrial assembly tools and Atlas Copco IAS product: SCA industrial dispensing systems
Atlas Copco Tools and Assembly Systems LLC
3301 Cross Creek Parkway
Auburn Hills, MI 48326 USA
+1 (248) 373 3000
Technical Support:
866.TOOL.FIX (866.866.5349)
SCA industrial dispensing systems +1 (248) 377 9722
Atlas Copco Henrob
30000 South Hill Rd
New Hudson, MI 48165 USA
+1 (248) 493 3800
Emergency & Technical Support:
+1 800 4HENROB (800 443 6762)
Contact us for Fabrication and Maintenance tools
Atlas Copco Tools and Assembly Systems
4428 Underwood Rd
LaPorte, TX 77571 USA
+1 (281) 448 5900