Technical Resource Library
Access comprehensive spec sheets, user manuals, certifications, and installation guides for the entire phasetwo cryogenic product line.
Product Documents and Manuals
Global Compliance & Certifications
PhaseTwo is committed to the highest standards of quality and safety. Our facilities and products are rigorously tested to meet global regulatory requirements for medical and laboratory environments
ISO 13485:2016
The global standard for Quality Management Systems in the medical device industry, ensuring every PhaseTwo product meets rigorous safety and efficacy requirements
EN ISO 13485:2016
Harmonized European quality standards for medical device manufacturing, confirming our compliance with EU-specific regulatory and safety frameworks
EU MDR 2017/745
Fully compliant with the European Medical Device Regulation (MDR), ensuring our cryogenic solutions meet the latest stringent requirements for clinical safety and performance.