Faster qualification
Include device category, target market, documentation needed, estimated volume and timeline to help Falkem evaluate the enquiry efficiently.
Medical devices
Falkem Swiss supports buyers looking for medical devices from qualified manufacturers, with attention to documentation, market requirements and practical supply follow-up.
Include device category, target market, documentation needed, estimated volume and timeline to help Falkem evaluate the enquiry efficiently.
Falkem Swiss is Swissmedic-authorised and treats documentation as part of the enquiry process rather than an afterthought.
About this category
Medical devices are regulated separately from medicinal products. Buyers sourcing for markets with formal regulatory frameworks typically need to confirm the device's classification, its CE marking or equivalent conformity-assessment documentation, and the relevant technical files or declarations of conformity. Falkem Swiss supports enquiries where buyers need to identify qualified manufacturers and obtain the available documentation for a specific device category.
When enquiring, useful details include the device category or type, the target market and its regulatory framework, the documentation you require and an estimated volume.
How we work
You tell us the product or project, target market and any documentation needs.
We identify and qualify the right sources under our Swissmedic GDP licence.
You receive a quotation with the supporting documentation available for that supply.
Supplies move through qualified logistics partners, coordinated end to end.
Active pharmaceutical ingredients from qualified sources.
Learn morePharmaceutical intermediates for chemical synthesis.
Learn moreFinished dosage forms from qualified manufacturers.
Learn moreNutraceutical brands meeting your market's control standards.
Learn moreOpen a prepared enquiry form for medical devices.