Device Specific Services

Timely Materials Screening

Safe devices for drug products

SAXOCON provides you with everything you need to test and document device compatibility with drug products in compliance with regulatory requirements.

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gas pathway

Breathing gas pathways

SAXOCON can help you to plan, test, and document compliance with regulatory requirements and get your gas pathway products ready for CE Mark certification.

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In vitro diagnostics

Safe in vitro diagnostics

SAXOCON helps you ensure that your in vitro diagnostic medical device complies with (EU) 2017/746 (IVDR) Annex I and is ready to be certified with a CE Mark.

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Stents and Implants

Safe stents and implants

SAXOCON can help you get your stents and implants ready for CE Mark certification. Our expert understanding of the ISO 10993-1 standard ensures that you are in good hands with SAXOCON.

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