CE Certification for Medical Device | EU MDR Regulation


HOTLINE: 0325269326

CE Marking Directives

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There are 23 product groups that are required to comply with the European standard directive CE Marking before entering the European market..

The CE regulation and directive means 'Compliance with European Standards for Products' according to a particular group.

CE certification is a standard regulation of the European Union (EU), which is allowed to circulate on the EU market.

CE certification is the "commercial passport" of products, opening up export opportunities to the EU market.

Won-Med provides CE certification services for businesses in Vietnam exporting to Europe.

Contact Hotline or send information to receive DETAILS PRICE LIST, SPECIFIC PROCEDURES FOR CE CERTIFICATION.

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Head Office in Korea: Rm512, Hanshin IT Tower, 272, Digital-ro, Guro-gu, Seoul, Republic of Korea.
Contact in Viet Nam: P7-43.OT09, Park 7, Vinhomes Central Park, 720A Dien Bien Phu St, Binh Thanh District, Ho Chi Minh City.

Tel: +84 (0) 283 620 6200 - Hotline: 0325269326.

Email: [email protected]

Website: wonmed.net

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