Clean room cleaning - Import export

Cleanroom bags and films - low-particle cleanroom bags and cleanroom films for research, pharmaceuticals, medicals Highest quality standards according to DIN EN ISO 14644, ISO 7, ISO 5 are fulfilled.

Pre-assembled assemblies for the clean room A kit consisting of parts that we have cleaned very finely is put together appropriately for clean room conditions and packed airtight. In this way, the assemblies can be brought directly to the appropriate production site without having to be unpacked or cleaned beforehand.

This high-end lift truck adhesive mat for cleanrooms and hygienic areas is a high-performance, antimicrobial mat or floor covering for walking on and light vehicles, such as lift trucks. This high-end lift truck adhesive mat for cleanrooms and hygienic areas is a high-performance, antimicrobial mat or floor covering for walking on and light vehicles, such as lift trucks. Reduced particle counts on the floor (up to 99.9%) and airborne particles (up to 75%) in critical areas.

A clean room is a controlled environment used for the production of very clean parts. starlim//sterner owns a clean room that meets the requirements of the following standards: ISO 14644-1 class 7 & 8 (defines the number of particles in the air) and GMP class C or D (defines the number of germs in the air). These silicone and 2-component parts are produced for the medical and the pharmaceutical industry. We also produce small and miniature parts for the automotive industry . The clean room incorporates the complete manufacturing process such as injection molding, post curing, washing and packaging of the molded parts. SHARE:

flexible coating as surface protection for concrete floor, decorative coating

International patent registered for the CLEAN ROOM SYSTEM line (DIN EN ISO 14644-1) The CLEAN ROOM SYSTEM units are linear actuators with belt driven transmission and are specifically designed for Clean Room applications They are supplied with a certificate issued by the IPA Fraunhofer Institute in Stuttgard, which certifies compliance with class ISO 3 (DIN EN ISO 14644-1), or with class Fed Std 0.01 (FED 209 E). The system prevents particles from being discharged in the environment where the linear unit is located. This has been achieved by using a special straight seal that closes the horizontal opening where the slider moves, as well as by the operation of a 0.8 vacuum pump connected to 2 vacuum pipes located inside the drive head and the idle head. The system allows vacuum to be generated inside the unit so that any particles released when the system is operating are sucked towards the air filtration areas. Clean Room System linear actuators components are all made of...

Our production is done in specifically equipped rooms, to rule out the possibility of product contamination from the outside. This includes, for example: special access authorisation, airtight walls and ceilings, windows that cannot be opened, air supply to the rooms being filtered, higher inside air pressure in relation to the outside air, insect lamps to prevent contamination with insects, mandatory protective clothing, shoe covers, gloves and hair covers, written authorisation with documentation for all work or events taking place in the rooms, such as cleaning, conversions, malfunctions. We have specialised in the particular needs of the pharmaceutical, food and health industries. All production takes place under clean room conditions and in compliance with the highest hygiene standards. Some sections are FDA-approved. Food additives are processed in accordance with the HACCP principles and in compliance with the European food hygiene directives and are prepared for dispatch.

We have been manufacturing UP machines / components and beam delivery systems for over 20 years.Benefit from our experience and let us do your demanding assembly or adjustment work.Assembly / adjustment of optical systemsAssembly / adjustment of mechanical precision systems.cleaning.Clean room assembly.Functional test.

ISO 14644-1 certified cleanroom with class 8 air cleanliness constructed by market-leading air system and cleanroom suppliers. We offer manufacturing of medical plastic bottles/components to packaging without human contact.

Pressteck is one of the world's leading specialists for deep-drawn individual parts on transfer presses and their processing into assemblies. In this non-cutting tension-pressure process, we produce hollow parts from a metal strip in several stages, which can be aluminium, stainless steel, copper or brass, among others. Compared to other processes, deep drawing has decisive advantages: Material consumption and production costs are lower, and at the same time the strength of the components is higher. We are highly innovative and optimise deep drawing technology beyond what is currently possible. We manufacture your individual component from coiled sheet metal and master demanding geometries and high degrees of forming.

These 60 x 90 cm permanent dust control sticky mats are an essential accessory for environments (e.g. cleanrooms) that require maximum cleanliness with foot traffic. Not only do they offer excellent particle binding, they are also easy to maintain and have a long service life of approx. 3 years. Permanently highly adhesive and easy-to-clean dust control mats made of high-quality silicone are the ideal solution for effective particle control on many types of flooring.

Pressteck has all standard sizes of MDI containers in its portfolio: 10ml, 14ml, 17ml and 19ml. If you need other sizes due to individual requirements, we are happy to offer these as well. Pressteck has all standard sizes of MDI containers in its portfolio: 10ml, 14ml, 17ml and 19ml. If you need other sizes due to individual requirements, we will be happy to offer you these as well. Depending on the medication and the propellant (CFC or HFA), different materials are used. We produce our containers from aluminium and stainless steel. While stainless steel containers are usually used uncoated, aluminium containers can also be offered in a coated version. Our containers are used as primary packaging for the administration of aerosol medication by inhaler. Patients worldwide use MDI (metered-dose inhalers) to treat respiratory diseases such as asthma and COPD.

The Multilift II clean has now been added to the range. It has been deliberately developed for use in the clean room. A special shroud for the DC motor with brushes of the lifting column means discharge of particles is kept to a minimum. To verify its suitability for use in clean rooms, the Fraunhofer Institute for Manufacturing Engineering and Automation IPA carried out a particle emissions test as per DIN EN ISO 14644-1 and certified the lifting column for use in clean rooms up to a globally valid class 4.

PEKUWhite - Our low-particle cleanroom films and cleanroom bags, tuned to your needs in the pharmaceutical, medicals, laboratory sector. The cleanroom packaging fulfils the highest quality standards.

The sampling bag SteriBag Cleanroom with double packaging can be placed directly in the clean room. 25 sample bags are placed in double secondary packaging. They can be removed one after the other and are therefore ideally suited for introducing into the clean room. Then the sterile bags can be used directly in the clean room. SteriBag Cleanroom is sterile inside and outside. This guarantees contamination-free storage and transport of solid, semi-solid and liquid media. The sample bag is perfect for use in chemical and pharmaceutical applications. The disposable sample bag has a labelling field, saves space and is also easy to transport. The large bag opening makes it easy to pour in the sample.

At a glance • PS, white • Optionally packaged individually and sterilised • With stripper edge • For single use • Clean room manufactured (clean room class 7) • Complies with EU food requirements and FDA regulations Volumetric and dosing spoons can be used to measure small amounts of powder, granulates and liquids exactly and dose them precisely. For precise measuring, excess medium is stripped off the upper edge of the spoon. The content volume is engraved on the handle. The flat front edge of the volumetric spoon is ideal for picking up medium from the bottom of the container or for getting into the corners of the container, thus allowing for good emptying of small remaining amounts. The flat base makes it possible to set the volumetric spoon down without spilling the content. The disposable dosing spoon is suitable for use as a sample spoon for taking small sample quantities.

For removing dust prior to maintenance and repair work, e.g. on magnetic plates, reading heads, audio-visual magnetic tape recording and playback heads, phonograph pick-ups, record turntables or phonograph records For cleaning vacuum sealing surfaces, sealing rings, high-voltage insulators, sample containers etc. For vacuum systems and device groups under clean-room conditions for semiconductor production Cleaning of opto-electronic reading units for bank checks and contactless cleaning of optical devices For maintenance of automated teller machines, quartz clocks or display panels For dedusting precision mechanical parts and assemblies in office machines, copiers, fax machines etc. Advantages and benefits Excellently suited for dedusting, blowing out and blowing off dust and liquids of all kinds Dry, oil-free compressed gas leaves behind no residues Replacement for ultrapure compressed air

The scan will generate a percentage that expresses the degree to which your current cleaning procedure meets the latest guidelines. You will also receive an overview per question, so you know exactly where improvements can be made.

AROUND CLEANROOM CLEANING A spotless cleanroom that meets stringent standards and guidelines is only possible by following the cleanroom cleaning regulations. TRU Cleanroom Cleaning offers companies with a cleanroom a free scan that focuses on fifteen points.

In addition to conducting a thorough audit of your cleaning procedures, we can also determine whether your team cleans according to the rules and regulations. This is essential to ensuring the sterility of your cleanroom. During the audit, the ultimate test will be determining the cleanliness of your cleanroom surfaces. Our PDL lights can detect particles up to 2 μm. We will compile the results of this on-site audit in a detailed report with concrete recommendations for improvement

During the audit, our experts will critically review your cleaning procedures and focus on all aspects that directly or indirectly influence them. They will present their findings and their recommendations in a clear and comprehensive report. This will give you a step-by-step plan for improving your procedures.

Did our Free scan determine that certain methods, techniques, or materials you use do not meet the industry standards? Do you want to know exactly which steps to take to comply with these rules? We would be happy to carry out a detailed audit.

You don’t just become a cleanroom cleaning expert overnight. The right knowledge and mentality are crucial for getting the job done right. This is even more true for our own employees. Following a strict selection procedure, an off-site training programme and a special on-site training programme, our new employees are ready to be deployed. All of our cleanroom cleaners receive an annual refresher course to update their knowledge.

Professional cleanroom cleaning is a true artform. It’s vastly different from standard cleaning and requires much more attention to detail. Why are the rules so strict? To guarantee the safety of your employees and the quality of your end product. The wrong cleaning technique, inadequate materials and outdated habits can potentially contaminate your cleanroom.

Outsourcing your cleanroom cleaning and disinfection to a specialised partner is highly recommended. However, if you prefer to use your own employees, we offer professional cleanroom cleaning training.

Besides continuity, TRU Cleanroom Cleaning offers you extensive expertise in clean-room and equipment cleaning. We train technical operators in accordance with the strict requirements of the pharmaceutical and biotechnical sectors and adopt the ‘Training Within Industry’ approach. Thanks to CEO Vanessa Morini’s years of experience , we are able to meet the most demanding equipment cleaning needs of the sector, both at a technical and chemical level. We ensure an efficient communication structure and we employ a proactive, strategic approach. Together, we strive to achieve the best possible result.

Vertalingen toevoegen equipment cleaning Sectors like the pharmaceutical and biotech industries are constantly growing. As a result, there is a huge demand for technical and scientific talent. At the same time, workloads continue to rise because of increasing complexity, production processes are changing ever more rapidly, and it has become harder and harder to find the right profiles. All this while operators are spending roughly 30% of their time carrying out repetitive tasks such as equipment cleaning. Why not outsource this job to a professional so your operators can focus on their core activities? This will allow you to boost your production capacity by up to 30%!

CROSS-CONTAMINATION This makes thorough cleaning of your equipment essential. Think of mobile tanks, filters, flexibles, centrifuges, reactors etc. We clean both the product contact side and the exterior of your equipment in accordance with the latest regulatory standards.

Our employees receive on-site guidance to ensure a flawless start. We monitor their work effort continuously and check the quality of their work and their documentation. We also have a trained back-up available for each employee, which enables us to meet all cleaning agreements and deadlines.