We prioritize customer safety and ensure that all our products comply with EU regulations. The General Product Safety Regulation (GPSR) is implemented by amending the Commodities Act. This amendment has taken effect on 13 December 2024.
Our products are classified as Class IIa medical devices under the EU Medical Device Regulation (MDR 2017/745) and are CE-marked for safety and quality assurance. Each product is tested for sterility and biocompatibility and comes with detailed instructions for safe use. If you have any questions regarding compliance, safety, or usage, please contact us at love@moepoplens.com
EU Responsible Person
MedPath GmbH
Country: Germany
Mies-van-der-Rohe-Strasse 8, 80807 Munich, Germany
G&G Contact Lens
93, Beoman-ro Suseong-gu, Beommul-dong, 401, 402 Beommul APT Type Factory, Daegu, Korea
EU Responsible Person
Shoujo Beauty
PO 51035 3007GA NetherlandsEdit