MALVERN, Pa. and STAFFORD, UK -- PuriCore, the life sciences company focused on the development and commercialisation of its novel, safe antimicrobial technology, announces that its Sterilox Endoscopy division has established a sales and marketing partnership with BHT Hygienetechnik GmbH, the award-winning manufacturer of endoscope reprocessors and channel checking systems.
This new partnership significantly enhances PuriCores product portfolio. The combination of award-winning technologies from Sterilox Endoscopy and BHT will deliver among the fastest and safest large pass through reprocessing systems in the UK. The deal ensures that PuriCore and BHT can respond to their clients need for high-quality infection control.
This deal follows last months announcement that PuriCore had signed an exclusive distribution agreement with Minntech Corporation, one of the worlds leading manufacturers of automated endoscope reprocessors.
PuriCore is pleased to announce another partnership with a world-class AER manufacturer, said Greg Bosch, chief executive officer of PuriCore. The integration of our technologies provides significant cost-saving benefits to our NHS customers and further strengthens our position as the UKs leading provider of endoscopy reprocessing systems.
"The joint effort allows BHT to expand its existing offerings in the UK market for high level disinfection solutions in the most sensitive field of reprocessing flexible endoscopes, said Dr. Annecke, CEO and managing director of BHT.
Source: PuriCore
The Sterile Processing Conference Survival Guide: How to Make the Most of Your Next Event
March 25th 2025From expert speakers to cutting-edge tools, sterile processing conferences, like the 2025 HSPA Annual Conference and the SoCal SPA's Spring Conference, offer unmatched opportunities to grow your skills, expand your network, and strengthen your department's infection prevention game.
Redefining Material Compatibility in Sterilization: Insights From AAMI TIR17:2024
March 24th 2025AAMI TIR17:2024 provides updated, evidence-based guidance on material compatibility with sterilization modalities. It offers essential insights for medical device design and ensures safety without compromising functionality.