Material
Stainless steel 1.4404 (316L) and other alloys approved for pharmaceutical use
Manufacturing
CNC precision machining on state-of-the-art equipment – tolerances in the micrometre range
Surfaces
Electropolished, pickled or fine-ground – Ra values to your specification
Certification
Material certificates, dimensional reports and roughness measurements as complete documentation
Precision for demanding environments
Pharmaceutical production places the highest demands on materials, surfaces and dimensional accuracy. Standard solutions frequently fail to meet these requirements. We manufacture bespoke stainless steel components and special tools matched exactly to your equipment and your GMP specifications.
What we manufacture
Special tools for pharmaceutical processes
Whether filling needles, closing tools, holding fixtures or equipment-specific aids – we develop and manufacture tools that fit your process precisely. Every part is made to your drawing or to a specification developed jointly with you.
Stainless steel components for cleanrooms
Cleanroom-compatible surfaces are not an option but an obligation. All our components are supplied with defined surface qualities – electropolished for optimum cleanability and minimised surfaces on which micro-organisms could be retained.
Retrofits and spare parts
Where original spare parts are no longer available or your equipment is to be upgraded, we manufacture matching components based on your actual dimensions – quickly, precisely and fully documented.
Materials and standards
- Stainless steel 1.4404 (316L) as the standard material for pharmaceutical applications
- Further alloys (Hastelloy, titanium) on request
- Surface quality Ra ≤ 0.8 µm electropolished as standard
- Complete material certificates to EN 10204 / 3.1
- Dimensional reports and roughness measurement included in the delivery
Quality assurance and documentation
Every component we manufacture is delivered with complete quality documentation: material certificate, dimensional report and surface certificate. These documents can be transferred directly into your QMS and form the basis for your qualification and validation files.