This certification is a significant milestone, marking COMAR’s compliance with the latest European Union medical device standards. The new EU MDR introduces more stringent requirements for the safety and performance of medical devices, seeking to ensure patient safety and device traceability. The successful certification demonstrates COMAR’s commitment to excellence and to bringing high-impact solutions to market, where they can positively impact the world around us.
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With this certification, COMAR can continue to sell CE-marked Oral/Topical Dispensing Devices in the European Union, specifically Class I devices with a measurement function and Class I non-measuring devices, which are press-in bottle adapters. The certification covers COMAR’s Oral Syringes, Dosage Cups (AccuCup®), Dosage Spoons, Dosage Scoops, and Dropper Assemblies.