Regulatory Requirements
DB Orthodontics ensures that its orthodontic and dental products meet the European Regulatory requirements detailed in MDD 93/42/EEC, as amended by Directive 2007/47/EC, the United States Medical Device Regulations (21 CFR Part 820) and the Canadian MDR (SOR/98-282) as applicable.
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As a member of the British Dental Industry Association, DB Orthodontics supports the industry’s Counterfeit and Substandard Instruments and Device Initiative (CSIDI). For more information and useful tips on spotting counterfeit dental devices visit the BDIA website.