Laboratoire Huckert's International

Laboratoire Huckert's International specializes in medical-grade products for high-level disinfection and reprocessing. Their portfolio includes disinfectant sprays (e.g., UMONIUM38® Neutralis Spray), liquid neutralising solutions (e.g., UMONIUM38® Neutralis 5L), pre-moistened medical tissues (e.g., UMONIUM38® Medical Tissues), and reusable medical instruments/probes (e.g., UMONIUM38® Probes). These products are designed for clinical environments where sterilization and disinfection are critical, such as hospitals and healthcare facilities.

The company is headquartered in Belgium, specifically in the region where its manufacturing and operational activities are conducted. This location aligns with its compliance requirements for EU medical device regulations.

Laboratoire Huckert's International’s devices are registered in the eudamed database, the official EU portal for medical device information. This registry ensures transparency and compliance with European Union medical device directives, allowing healthcare professionals and regulators to verify the company’s products.

The company’s products fall under Class IIa and Class IIb classifications according to the EU Medical Device Regulations. This classification is determined by factors like the intended use (e.g., disinfection, reprocessing) and associated risks. Class IIa devices pose a moderate risk, while Class IIb devices carry a higher risk, necessitating stricter regulatory oversight to ensure safety and efficacy.