US FDA/ UL approval

The Medical Devices Directive (93/42 EEC) for example, requires foreign manufacturers (not established in the EU) to utilize an Authorized Representative as liason between the Competent Authorities, the foreign Manufacturer, and the Manufacturers' Customers to assure timely and complete access and required information exchange. Walt Medical LTD can provide almost any level of service required to meet the regulations of your target country(s) - compiling and maintaining your technical file, for registrations and filings, or basic or intensive Customer Communication and Vigilance. Please see the Services links for details.

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