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Secondary packaging for medical devices

Looking for a subcontractor who can handle the secondary packaging of your medical devices?

Cemiplast handles the secondary packaging of medical devices in Switzerland, in addition to production and primary packaging. You receive a ready-to-distribute product.

Managing secondary packaging of medical devices downstream of production

Packaging management is one of the steps Cemiplast handles after production and assembly of the parts. Secondary packaging then protects and groups devices already in primary packaging, before shipment.

ISO
0
certification covering processes and products

Secondary packaging of medical devices: a continuous production chain

By centralising production, assembly, primary and secondary packaging, Cemiplast limits handling breaks and transfers between subcontractors. This is a traceability issue for medical device manufacturers.

Secondary packaging of medical devices also carries the regulatory labelling and batch-by-batch traceability. It is part of Cemiplast’s ISO 13485 quality system, which makes tracking easier through to the end customer.

Cemiplast can also design the primary packaging at the same time as the part, directly in an ISO 7 cleanroom. The move to secondary packaging then happens without changing supplier.

Technical specifications of secondary packaging for medical devices

Certification

ISO 13485

Location

Saint-Imier, Suisse

Presse d'injection plastique en salle blanche ISO 7 pour dispositifs médicaux, dispositifs dentaires, micro-pièces techniques, IQ OQ PQ, industrialisation, production, assemblage, conditionnement, contrôles, conception et développement de pièces plastiques, conception de packaging primaire, atelier de Saint-Imier en Suisse

How we work with you

Initial discussion

Initial literature search and assessment of the patentability of the idea, to frame the project.

Design and development

Part design, taking into account the functional, economic and regulatory constraints of the project.

Prototyping

Prototype pre-production, to validate the material choice and feasibility before industrialisation.

Industrial phasing and production

Industrial phasing then production of the moulded parts, with assembly depending on the project.

Packaging and validation

Packaging development, packaging management and process validation.

They trust us

Medical device manufacturers entrust Cemiplast with the entire chain, from production to secondary packaging.

Frequently asked questions about secondary packaging for medical devices

Yes. Cemiplast handles secondary packaging in addition to production and primary packaging. You receive a ready-to-distribute product.

Centralising these steps at Cemiplast reduces transfers between suppliers. It also makes traceability easier, an important issue for medical devices.

Yes, labelling and batch-by-batch traceability are part of Cemiplast’s ISO 13485 quality system, applied to secondary packaging.

Secondary packaging protects and groups devices already in primary packaging, before shipment.

Yes. Secondary packaging is part of Cemiplast’s ISO 13485 quality system, which covers processes and products.