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About us
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Overview contacts order processing
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Technical
Medical
Chemical
Materials
Partners
CleanControlling North America
About
Products and Services
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Extraction System C|PS
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A focus on particles, Technical Cleanliness
Standard cleanliness inspection / residual particle contamination analysis
CCPlus - Cleanliness inspections for increased blank value requirements
Cleanliness inspections of large components
Cleanliness inspections by means of through-flow air extraction
Cleanliness inspections by means of suction extraction
Design and manufacturing of test adaptations
Material determination of inorganic particles - SEM/EDX analysis
Material determination of organic particles - IR spectroscopy
Chemical-filmic component cleanliness
AGREE® - gravimetrically detectable residues (µNVR) by means of nanobalance (QCM)
Gravimetric determination of non-evaporable residues (NVR)
Determination of the surface tension
Determination of organic compounds (IR)
Qualitative and quantitative determination of ionic residues (IC)
Determination of the conductivity of residues (ROSE)
Determination of the water-soluble total organic carbon (TOC)
Characterization of unknown impurities
Fluoride and residual pollution test
Determination of filmic impurities - greases, oils, processing auxiliaries (GCMS)
Determination of filmic contamination - practical examples
Particle purity of oils, lubricants
Particle contamination in oils
Testing of lubricating greases
Products
C|PS - Suction extraction system
C|PS - Particle suction extraction
C|PS - Particle Separation
C|PS³apex - complete system with digital control
C|PS² - compact system
C|PS - Features
C|PS - Application examples
C|PS - Service
C|PS - Application videos
Product catalogue
Particle trap
Particle stamp
Consulting
Consulting - Battery Cells
Consulting - HV Vehicle Batteries - Part 1
Consulting - HV Vehicle Batteries - Part 2
Consulting - HV Vehicle Batteries - Part 3
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Testing methods
Determining the decay curve
Analysis filtration
Ultrasonic extraction
Air throughflow extraction
Air jet extraction
Suction Extraction
Gravimetry
Microskopy
Magnetism on surfaces
Residual oil/Residual grease
Oil analyses ISO 4406
Test standards
VDA 19
ISO 16232
ZVEI Guidline Technical Cleanliness
Guidline VDI 2083 Page 21 - Cleanliness of medical devices in the manufacturing process
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Biological analytics
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End-of-life simulation reprocessing cycles
Hygiene / Hospital Hygiene
Chemical analytics
Chemical characterization - DIN EN ISO 10993-18
Toxicological evaluation - DIN EN ISO 10993-17
Unknown substances
Particle analytics
Particle contamination of medical devices
Material identification of particles
Analytics of AM products
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Testing methods
Bioburden Determination
In vitro cytotoxicity test
Endotoxin test
TOC Determination
THC Determination
Norms and Standards
Bioburden
Cytotoxicity, biocompatibility
Endotoxin test (LAL test)
TOC determination of water-soluble organic contaminants
Particles in medical technology
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