Laboratory Research Equipment
Shop ECOLAB Sekusept Pure Clean instrument-cleaning products by exact reference for professional medical-device decontamination and validated reprocessing workflows.
The category currently contains two ECOLAB Sekusept Pure Clean references. Confirm the precise pack and formulation details before ordering, then use only within the validated reprocessing procedure for the device.
ECOLAB instrument-cleaning product listed under reference 3080920. Verify the current pack size, format, dilution and manufacturer instructions.
Alternative ECOLAB listing under reference 3080940. Do not assume it has the same pack configuration as the other catalogue reference.
Confirm the reusable device manufacturer permits the cleaner, concentration, temperature, immersion method and processing equipment.
Prepare the working solution using the stated product quantity, water volume, water quality and temperature for the approved process.
Use the validated exposure time and cleaning action. Disassemble, open, flush or brush devices only as directed by their instructions.
Complete the specified rinse, dry and visual-inspection stages before the device proceeds to disinfection, packaging or sterilisation.
Instrument cleaning is one stage of reprocessing. The product, device and local procedure must agree before the chemical is introduced into the workflow.
| Check point | What to record | Why it matters |
|---|---|---|
| Catalogue identity | 3080920 or 3080940, product name, pack size and batch | Prevents the two Sekusept listings or pack configurations being treated as interchangeable |
| Device compatibility | Manufacturer, model, materials, lumens, joints and reprocessing limitations | Protects the device and keeps processing within its validated instructions |
| Solution preparation | Concentration, water volume, water quality, temperature and preparation time | Ensures the working solution is prepared consistently and traceably |
| Cleaning process | Pre-treatment, disassembly, immersion, brushing, flushing and exposure time | Supports removal of contamination from accessible and internal surfaces |
| Solution management | Maximum use period, visible soil, testing requirements and replacement criteria | Prevents continued use outside the approved working conditions |
| Post-cleaning stages | Rinse method, drying, inspection result and subsequent disinfection or sterilisation | Confirms the item is ready to move safely to the next validated process stage |
Effective cleaning depends on consistent preparation, complete access to contaminated surfaces and a traceable handover to later reprocessing stages.
Prevent avoidable drying of contamination and transport devices in line with the approved local procedure.
Open, disassemble and flush devices only as required by their current reprocessing instructions.
Record preparation, exposure, solution replacement and inspection information required by the quality system.
Apply COSHH controls for PPE, ventilation, splashes, spills, storage and safe chemical disposal.
Providing the complete reference and process context helps distinguish the two catalogue listings and supports accurate product identification.
Include 3080920 or 3080940, the required pack description and a photograph of the current packaging where available.
Confirm the reusable-device family, materials, cleaning method, working concentration and relevant approved procedure.
Provide the required quantity, estimated usage, delivery deadline and whether the enquiry supports routine CSSD stock or a new process.
Our sister websites also cover ECOLAB healthcare cleaning and professional instrument-decontamination products. Availability and pricing may differ by website.
View the related ECOLAB category for professional instrument cleaning, decontamination and sterile-services procurement.
Visit Aston Pharma →Browse complementary cold-processing and reusable-instrument decontamination products for professional infection-control workflows.
Visit Medical World →It is listed here as a professional cleaner for approved medical-instrument reprocessing workflows. Suitability must be confirmed from its current manufacturer information and the reusable device's instructions.
The live category lists both references but does not clearly state the pack distinction. Confirm the current product description, pack size and formulation before ordering rather than assuming they are equivalent.
No. Cleaning removes contamination and supports later stages, but the complete validated process may also require disinfection and sterilisation according to the device, intended use and local policy.
No universal compatibility should be assumed. Confirm materials, construction, device manufacturer instructions, ECOLAB information and the validated local procedure.
Use only the concentration, water volume, water quality, temperature and preparation method stated in the current instructions and approved procedure. Do not estimate or mix by appearance.
Send the complete ECOLAB code, current pack details, device family, cleaning method, working concentration, required quantity and a clear packaging photograph if available.
Send us reference 3080920 or 3080940, the current pack description, device family, required quantity and delivery timescale. We can help locate the relevant catalogue listing.
