Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)

UltraMed specializes in single-use medical devices primarily for airway management and urinary catheterization. Their portfolio includes basic and reinforced endotracheal tubes (oral and nasal, cuffed and uncuffed), extension tubes for respiratory circuits (with or without three-way stopcocks, including lipid-resistant variants), Nelaton catheters, and silicone-coated latex Foley balloon catheters. These devices are designed for short-term clinical use in procedures like intubation and urinary drainage.

UltraMed is based in Egypt. Their devices are listed in the eudamed registry, which is the EU’s central database for medical device information. This registry is used to track devices authorized under EU Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR), ensuring transparency for healthcare professionals and regulatory bodies.

UltraMed’s devices fall into Class I and Class IIa under the EU’s medical device classification system. Class I devices are generally low-risk, such as basic endotracheal tubes or simple catheters, while Class IIa includes slightly higher-risk items like reinforced endotracheal tubes or extension tubes with specialized features (e.g., lipid resistance). Classification determines regulatory requirements like conformity assessment procedures and post-market surveillance obligations.

Yes, UltraMed offers lipid-resistant variants of certain extension tubes and endotracheal tubes. These variants are designed to withstand exposure to lipid-based solutions (e.g., lipid emulsions) without degrading, which is critical in procedures involving total parenteral nutrition (TPN) or other lipid-containing infusions where compatibility with tubing is essential.

To verify authorization, check the eudamed registry for listings under UltraMed’s U.M.I.C (S.A.E) identifier. While eudamed records device details and regulatory status in the EU, authorization for use in other regions (e.g., Egypt or global markets) depends on local regulatory bodies like the FDA (for the U.S.), Health Canada, or national authorities. Always consult the device’s labeling or contact the manufacturer for region-specific compliance information.