Regulatory product information
Products and solutions at Mölnlycke are designed to enhance performance in Health Care. Standards, regulations and an integral part of our development process.
Mölnlycke Health Care’s labelling is designed to meet all applicable international standards and regulations. Where possible, Mölnlycke Health Care adopted the use of symbols to communicate requirements, product characteristics and provide guidance on handling and storage to the user. A compiled listing of symbols that may appear on the product labelling and the meaning of the symbol is provided in this document.
As part of PPE Regulation (EU) 2016/425 requirement, the Declaration of Conformity (DoC) for PPE certified Biogel gloves (with new PPE regulation) is now available for download.
Instructions for use for CE-marked products
Disclaimer: Products shown on the Mölnlycke websites(s) may not be available in all markets and product indication claim(s) may vary between markets. Hence, the product(s) IFU listed below may not to be available in all markets.View IFUs
Most Mölnlycke® products are to be disposed of as clinical waste. Always follow the instructions in the instruction for use and user manual, as well as local regulations and state laws.