Portal and digital medical technology fair of the largest MedTech cluster in Germany
The forum participants showed great interest in the diverse topics and the exhibiting companies.
CleanControlling Medical was able to use this opportunity to answer a wide range of questions, for example on determining the biocompatibility of materials and medical devices - in particular their chemical characterization. The validation of the final cleaning of medical devices is also a core topic on which the participants were able to exchange expert information.
To the original article
Und: Warum sie nichts mit der ISO 10993 zu tun haben.
And: Why they have nothing to do with ISO 10993.
Definition, procedure, and tests
Learn more about definition, procedures and tests according to DIN EN ISO 17664-1/-2 and DIN EN ISO 17665
What does this mean and what is the difference to validation of reprocessing according to the manufacturer's instructions? What analyses are typically...
Basics, methodology and significance
Limit values, detection methods and test strategies - Or: What do horseshoe crabs have to do with endotoxins?
Particle analyses of medical devices
Optical particle counter (OPC) or microscopic evaluation?
Materials testing: Quality testing of metal bar material
Differences, advantages and disadvantages of ultrasonic and CT testing in the quality inspection of metal bar material
Importance and Limitations of the TOC analyisis
Influences of the sample composition
Cytotoxicity tests on medical devices
Important aspects of cytotoxicity tests on medical devices: Parameters, extraction and incubation times and evaluation methods.
CleanControlling Medical GmbH & Co. KG
Gehrenstraße 11a
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