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“The medical device manufacturer VDW GmbH is certified according to EN ISO 13485:2016. The company’s marketable products are fully subject to the regulatory provisions of Council Directive 93/42/EEC of 14 June 1993 on medical devices and bear the corresponding CE marking.
Within the framework of the corresponding requirements, all materials used by the company are also secured and checked in accordance with Regulation (EC) no 1907/2006. In accordance with the product design, the finished products are also validated for safety and efficacy and the corresponding labelling is made available to the user/customer, in line with labelling regulations. Based on the applicable requirement, the manufacturer is not subject to any further provisions according to (EC) no 1907/2006 (2) safety data sheets for finished products.”
VDW is certified manufacturer of medical devices according to 93/42/EEC.
VDW EG Certificate G1 (valid until 2024.05.26)
VDW EG Certificate G2S Sterile Root Canal Instruments (valid until 2024.05.26)
VDW ISO13485:2016 (valid until 2022.05.26)
MDSAP Certificate (valid until 2022.04.17)