KEELER

The primary goal of Keeler is to prevent vision loss by making safe, legal, and high-quality medical devices available to our customers and clients. keeler products meet all applicable regulatory requirements, including UK Medical Device Regulation 2002, Medical Device Directive 93/42/EEC, and Medical Device Regulation 2017/745. By affixing the CE and UKCA markings to our products, we certify that they are safe and meet all requirements for environmental, health, and safety. certifications include ISO 13485:2016, ISO 14001, Medical Device Single Audit Programme (MDSAP), UKCA and CE.