GrowthImports is an ISO13485 certified medical device importer that assists medical device manufacturers in expanding their reach in the European and UK market. We provide financial and importing services tailored to the needs of our customers to maintain an efficient operation and ultimately contribute to their growth.
One stop shop for your growth needs
GrowthImports was founded due to the changes in the Medical Device Regulation and the need for medical device manufacturers to have one dedicated solution to ease market access in the EU and UK market efficiently. With over 30 years of combined experience in medical device regulations and market development services exclusively for medical device companies, our approach differentiates by our expertise, custom and personal approach. Our goal is to guide and support our clients so they can reach their international goals faster with more success. GrowthImports is the sister company of GrowthMedics, an organisation that focuses on global market development services.
Growth is determined by the success of people. Our international growth team is passionate, knowledgeable, and dedicated to our clients’ growth.
Our skin in the game approach and turnkey range of growth services are aligned to meet our clients’ global growth objectives – together we will build the best suitable growth plan.
Overcome cultural and operational barriers such as time zone, logistics, regulations, language, culture or having the right stakeholder network.
Increase your speed to market time by leveraging our growth infrastructure and capabilities in the global patient and hospital equipment industry.
Save time and minimize risk, costs, and liabilities involved by avoiding setting up a physical presence or hiring your own full-time staff.
Our range of growth services are all designed to address the international growth needs of worldwide medical device companies, from early to late expansion.
Visit our resource section for the latest news, white papers and blogs about the global medical device industry
If you are a non-EU manufacturer, you must comply with the Medical Device Regulation (MDR). The Regulation states that manufacturers must select an importer to
The instructions for use (IFU) pertaining to medical devices substantially differ between the Medical Device Regulation (MDR) and the Medical Devices Directive (MDD). Despite the
The CE Mark is mandatory for medical devices Imported to Europe. Learn how your products can get CE marking based on Medical Device Regulations. When