Clean room assembly

Clean room assembly

Clean room assembly

Medical products are subject to enormous requirements in terms of hygiene and purity.
We are aware of our responsibility for products that later serve the health of humans and animals.


And we have more than 30 years of experience in cleanroom production. Regular particle and germ measurements ensure purity.


The entire production chain can be offered from laminar flow to ISO Class 8 clean room conditions, depending on requirements.


In addition to 21 fully automated assembly machines, we offer our customers customized assembly concepts—whether manual, semi-automated, or fully automated.
We offer a high degree of manufacturing flexibility – from prototypes to series production.


Upon request, even large quantities can be produced, processed, and assembled under clean room conditions.


So we know what we’re talking about – and offer flexible solutions, whether in production, assembly, or packaging.

Clean room assembly
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Satisfaction

  • Monitored and controlled cleanroom conditions - in accordance with ISO Class 8
  • Purity of laminar flow up to class 10,000
  • 300 square meters of production space
  • Automated assembly with camera monitoring and manual assembly of complex assemblies
  • Adhesive bonding technology for plastic pens
  • Various sterile packaging (welding + sealing, ultrasonic welding)
Additional services:
Advantages

Your Advantages with Us!

Innovative

Forward-looking
solutions for medical technology

Competent

100 years of expertise for products you can rely on.

Individual

Customized
products that perfectly match your requirements.

Qualitative

Precise products of the highest quality – certified and reliable.

More information about cleanroom assembly

We understand our customers’ high demands for maximum safety and cost-effectiveness combined with short turnaround times. To meet these requirements, we combine all the necessary joining and testing technologies in one efficient, coordinated process. Our range of services extends from manual to semi-automated and fully automated assembly systems.


Our assembly processes are verified both inline and downstream by a variety of tactile and optical testing methods, leak tests, and 100% camera inspections. This enables us to ensure consistently high assembly efficiency in small and large series while also guaranteeing complete traceability of all relevant process steps.


In addition to our assembly services, we offer standardized and customized packaging solutions for every batch size. These meet all requirements for hygiene and counterfeit protection and comply with industry-specific legal requirements as well as individual customer specifications.

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Process

Our Approach

1. Consultation

Benefit from individual advice and tailor-made solutions, perfectly tailored to your projects. Our precise choice of materials meets the highest technical requirements and ensures optimal results.

2. Design

Working closely with you, we develop customized products that are tailored precisely to your requirements. Each solution is thoroughly tested to ensure maximum functionality and the highest quality standards.

3. Production

Through close cooperation, we develop customized products that are precisely tailored to your needs. Each solution is extensively tested to ensure maximum functionality and quality.

4. Delivery

Our on-time delivery guarantees you fast and reliable delivery. With our reliable after-sales service and long-lasting product functionality under all conditions, you will benefit from the highest quality in the long term.

Common problems

1. Strict regulations and approval hurdles: Medical technology is subject to comprehensive legal requirements and demanding approval processes. Many providers lack the necessary expertise to prepare and release products for market entry quickly and in a targeted manner.

2. Lack of material expertise: Choosing the right material is crucial. Without a deep understanding of biocompatible plastics and the specific requirements of medical applications, product safety and quality can be jeopardized by wrong decisions.

3. Delayed market launch: A lack of precise development processes and rapid prototyping delays market access, resulting in missed opportunities, rising costs, and a competitive advantage for rivals.

Our solutions

1. Expertise in regulatory matters: Thanks to our many years of experience and comprehensive knowledge of legal requirements, we ensure that your product receives all necessary certifications quickly and reliably. We take care of conformity assessment and documentation – CE.

2. Material expertise & innovative strength: We carefully select the optimal materials that guarantee maximum safety, performance, and durability. Every raw material used is tested in practice and documented in accordance with standards—this enables us to guarantee legally compliant, efficient, and scalable production.

3. Rapid prototype development: With the help of efficient development processes and state-of-the-art manufacturing technologies, we are able to provide functional prototypes in a short period of time. This shortens the time to market and reduces potential risks.

FAQ

Frequently asked questions

What are the main advantages of cleanroom assembly compared to other solutions?

Cleanroom assembly offers numerous advantages over conventional assembly methods. Particularly noteworthy are the significant reduction in particles and contamination, the ability to meet the most stringent quality requirements, and the increase in product reliability and service life. This makes cleanroom assembly particularly suitable for industries such as medical technology, semiconductors, and pharmaceuticals.

As a customer, how much influence do I have on the development process for cleanroom assembly?

As a customer, you are actively involved in the development process. Your requirements and wishes are taken into account in close consultation with you. You have the opportunity to influence the entire planning and implementation process, submit change requests, and help shape progress.

What factors influence the cost of clean room assembly?

The costs for cleanroom installation are calculated individually. Important factors include the scope of the project, the desired functions, the cleanroom class, specific customer requirements, and the objectives to be achieved. Since every task is unique, it is not possible to give a flat-rate price. However, we would be happy to provide you with a customized quote based on your specifications.

What kind of support and assistance is available after the project is completed?

Once the clean room assemblyinstallation project has been completed, we offer comprehensive support and assistance. This includes regular maintenance, technical support, rapid troubleshooting, spare parts service, and advice on optimizations and expansions. Our customer service team is also available to you as a long-term point of contact.

How long does it take to complete clean room assembly?

The duration of a clean room assembly installation project depends on the scope of the project and the specific requirements. Typically, such projects take around four weeks to complete. In individual cases, the time frame may vary, but we will always keep you informed about the planned time frame in a transparent manner.

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