Who Needs to Comply?
Overview
MedDO assigns specific obligations based on your role in the supply chain. The four primary roles are manufacturer, CH REP, importer, and distributor.
| Role | Established in Switzerland? | Conformity Assessment | DAPI Registration | Vigilance Reporting |
|---|---|---|---|---|
| Manufacturer | Not required | Yes (primary responsibility) | Yes (or via CH REP) | Yes (primary) |
| CH REP | Required | No (assists) | Yes (on manufacturer's behalf) | Yes (assists) |
| Importer | Required | Verify only | No | Report to manufacturer/CH REP |
| Distributor | Not required | Verify only | No | Report to manufacturer/CH REP |
Manufacturer
Responsible for ensuring device compliance, QMS, technical documentation, conformity assessment, declaration of conformity, and post-market obligations. Non-Swiss manufacturers must appoint a CH REP before placing devices on the Swiss market. See Manufacturers.
Swiss Authorised Representative (CH REP)
Mandatory for non-Swiss manufacturers. Performs or assists with Swissmedic registration, vigilance reporting, FSCA coordination, and inspections. Jointly and severally liable with manufacturer. See CH REP.
Importer
Any natural or legal person established in Switzerland who places a non-Swiss manufacturer's device on the Swiss market. Must verify conformity, labelling, and CH REP appointment. See Importers and Distributors.
Distributor
Makes a device available on the Swiss market without being the manufacturer or importer. Must verify labelling and cooperate with surveillance activities.
Official Sources
Content is AI-assisted and intended as a navigation aid only. Always verify against official Swissmedic and Fedlex sources. Not legal or regulatory advice.