Scroll down to view or download supporting documentation for Keeler products, translated for key global markets.
Click on the link to go straight to product brochures and cleaning instructions, Instructions for use (IFU) manuals, and ISO certificates below:
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.
Our 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. Our certifications include ISO 13485, ISO 14001, Medical Device Single Audit Programme (MDSAP), UKCA and CE.
