Why it matters
Particulate contamination can lead to increased wear, malfunctions or failures. Requirements are increasing, especially in automotive, e-mobility, mechanical engineering and medical technology.

Basics and selection
Assessing and securing technical cleanliness according to VDA 19.1, ISO 16232 and OEM and customer factory standards. Find out which test fits your component.
Technical cleanliness describes the control and assessment of particulate contamination on parts, assemblies and technical systems. Even the smallest particles can impair the function, reliability and service life of sensitive components.
Particulate contamination can lead to increased wear, malfunctions or failures. Requirements are increasing, especially in automotive, e-mobility, mechanical engineering and medical technology.
Systematic cleanliness testing helps detect potential risks early and derive suitable measures for process optimisation.
The specification for your component is usually on the drawing, the purchase order or your customer’s factory standard.
Inspection of technical cleanliness of functionally relevant automotive components. Accredited to the 2015-03 edition (E.1 to E.4, F.1 to F.3); a 3rd edition has been available since 2026.
VDA 19.1 residual contamination analysisCleanliness of components and systems of road vehicles, 2018 edition. Does not define limit values. Accredited excluding the methods of clauses 9.3 and 9.4.
ISO 16232 cleanliness analysisIn addition to VDA 19.1 and ISO 16232, TecClean regularly carries out residual contamination and cleanliness analyses according to OEM, factory and customer test specifications. Many of these manufacturer-specific requirements are methodically based on the principles of technical cleanliness according to VDA 19.1 or ISO 16232 and are implemented according to the applicable test specification.
More on factory standardsCovers environment, logistics, personnel and assembly equipment. For context; components are tested according to VDA 19.1 or ISO 16232.
Extraction removes the particles from the component. They are then collected on an analysis filter and evaluated.
Customer-specific methods or methods developed by TecClean are also possible. They are not automatically part of the scope of accreditation. If required, further analyses such as SEM/EDX or FTIR can be coordinated through an accredited partner laboratory.
In addition to VDA 19.1 and ISO 16232, TecClean regularly carries out residual contamination and cleanliness analyses according to OEM, factory and customer test specifications. Many of these manufacturer-specific requirements are methodically based on the principles of technical cleanliness according to VDA 19.1 or ISO 16232 and are implemented according to the applicable test specification.
Send us the factory standard, drawing or test specification that applies to your order. TecClean checks feasibility and the necessary test scope and agrees the next steps directly with you.
Residual contamination analysis according to the stated specification.
VDA 19.1Cleanliness analysis according to ISO 16232.
ISO 16232Decay measurement to define the extraction parameters.
Decay measurementExpress after technical consultation.
Express serviceSend a filter, membrane, stamp or tape-lift.
Filter evaluationHave bath samples and process media analysed.
Bath samplesFour steps to your test report
Share the component, drawing, limit value, standard or customer requirement.
Together with you, TecClean determines which test scope is required and technically feasible.
Send the sample or test lots to TecClean, securely packed.
TecClean carries out the agreed analysis and provides the test report.
For suitable parcel-sized samples: optional express processing within 1 to 2 working days. The day of delivery is not counted.
FAQ
Technical cleanliness describes the control and assessment of particulate contamination on parts, assemblies and technical systems.
In a residual contamination analysis, the particles are removed from the component with a suitable extraction method, collected on an analysis filter and evaluated gravimetrically and microscopically. The result is documented in the test report.
For example spraying, rinsing, shaking, ultrasound, air extraction and stamping, using suitable solvents or deionised water. The annex to the accreditation certificate states which methods are accredited.
In addition to VDA 19.1 and ISO 16232, TecClean regularly carries out residual contamination and cleanliness analyses according to OEM, factory and customer test specifications. Many of these manufacturer-specific requirements are methodically based on the principles of technical cleanliness according to VDA 19.1 or ISO 16232 and are implemented according to the applicable test specification.
We support you in assessing parts, processes and cleanliness specifications and in implementing customer and OEM requirements.