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Medical plastic injection moulding
Looking for a medical plastic injection moulding subcontractor in Switzerland?
Cemiplast designs and manufactures plastic parts for medical devices, dental devices and their packaging. The company has been ISO 13485 certified since 2016 and operates two ISO 7 cleanrooms in Saint-Imier, Switzerland.
Why medical plastic injection moulding requires a specialist partner
A medical or dental device manufacturer remains responsible for the compliance of its subcontractors, from meeting the European MDR to the traceability of every batch produced.
Entrusting injection moulding to an ISO 13485 certified partner with qualified cleanrooms reduces this risk from the part design stage. It also makes supplier audits easier, whatever the type of device or packaging.
At Cemiplast, medical plastic injection moulding takes place in two ISO 7 classified cleanrooms. This cleanliness class is more demanding than ISO 8. It covers the moulding, assembly, inspection and packaging of your parts.
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injection moulding machines
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ISO 7 cleanrooms
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-100T
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ISO 13485 certified
Our areas of expertise in medical plastic injection moulding
Our approach to medical plastic injection moulding
Cemiplast builds regulatory requirements into the part from the design stage. Its multidisciplinary team is used to developing medical devices to the ISO 13485 standard. It also knows the requirements of the European MDR.
Cemiplast’s specialities in medical plastic injection moulding are technical micro-parts, multi-shot parts and insert overmoulding. Thanks to micro injection moulding, some components weigh less than a tenth of a gram, with very tight tolerances.
Depending on your needs, Cemiplast handles part design, prototypes, industrial phasing and production. Assembly, primary packaging, packaging operations and process validation complete the service. The move to series production is detailed on our industrialisation page.
They trust us
Industrialisation of two automated production lines for endodontic irrigation cannulas
Development of the moulding technology for a subcutaneous micro-cannula, from prototype to pre-series
Insert overmoulding for contra-angles, moulding of technical micro-parts
Cemiplast manufactures moulded parts for Produits Dentaires SA (PDSA), whose injection solutions are listed on PDSA’s 360° Injection Solutions page.
Frequently asked questions
Cemiplast works on medical devices, dental devices and their primary and secondary packaging, with the same requirements for traceability and ISO 13485 compliance.
Cemiplast has been ISO 13485 certified since 2016 and has two ISO 7 cleanrooms, two requirements that medical device manufacturers commonly ask of their subcontractors.
Cemiplast masters micro injection moulding, multi-shot parts and insert overmoulding. Some of its micro-components weigh less than a tenth of a gram.
Cemiplast’s ISO 7 cleanrooms combine moulding, assembly, inspection and packaging. These processes are adapted to the requirements of each project.
Yes. Primary packaging development and packaging management are among the steps Cemiplast handles.