New swissdamed registration fees - what manufacturers need to know from 2027

From 1 July 2026, all medical devices placed on the Swiss market must be registered in the national swissdamed database. Together with this registration obligation, the Swiss Federal Council has approved a revised Swissmedic fee ordinance introducing a product registration fee. The first invoices will be issued in January 2027. Here is what to expect.

MedNet EC-REP

Author

15. Juni 2026

MedDOIvDOSwissdamedCH-REP

Background: the swissdamed database

swissdamed is Switzerland's national medical device database, managed by Swissmedic. It ensures traceability of products on the Swiss market and is part of Switzerland's gradual alignment with the European MDR/IVDR regulatory framework. Registration in swissdamed became mandatory on 1 July 2026, with a transitional period running until 31 December 2026.

The new fee structure from 2027

The Federal Council has approved a revision of the Swissmedic Fees Ordinance introducing a product registration fee. The fee is designed to cover the administrative costs that device registration in swissdamed generates for Swissmedic.

The fee structure is as follows:

First product registration (UDI-DI) per year: CHF 200
Each additional product registration (UDI-DI) per year: CHF 20
Maximum per manufacturer per year: CHF 10,000

In practical terms: from the 492nd registered product onward, no further fees apply.

Who pays - and when?

The cutoff date for the first fee calculation is 31 December 2026. All UDI-DIs carrying the status "on the market" in swissdamed on that date will be included in the first invoice run in January 2027. Ongoing invoicing for new registrations will follow on a rolling basis, with each new calendar year triggering a fresh fee calculation.

One important point: fees are charged per manufacturer, not per CH-REP (Swiss Authorised Representative).

What this means for your swissdamed registration

Correct maintenance of product status in swissdamed is now directly linked to your fee exposure. Products that are no longer placed on the Swiss market should have their status updated accordingly before the 31 December 2026 cutoff to avoid unnecessary charges.

Checklist for manufacturers:

All products currently on the Swiss market registered in swissdamed in time?
Product statuses correctly maintained - especially "on the market" vs. no longer marketed?
CHRN (Swiss Single Registration Number) obtained for all relevant economic operators?
Invoicing address and contact details with Swissmedic up to date?

How MedNet supports you

As your CH-REP, MedNet EC-REP guides you through all swissdamed registration requirements. We register your products and maintain your product data correctly and prepare for the new fee structure before the December 2026 deadline.

If you have questions about your Swiss product portfolio or swissdamed registration, please reach out to us directly.

Sources:
Swissmedic — Registration fee
Swissmedic — Federal contribution increased

erstelle ein bild auf dem keine personen abgebildet werden. Das bild muss zu diesem Artikel passen: eIFUs – How to benefit as professional-use device manufacturer?
EU Expands eIFU Eligibility for Professional-Use Devices under Commission Implementing Regulation (EU) 2025/1234
The regulatory framework for electronic Instructions for Use (eIFU) in the European medical device sector continues to evolve. With the adoption of Commission Implementing Regulation (EU) 2025/1234, the European Commission has expanded the categories of medical devices that may provide instructions for use in electronic form (https://eur-lex.europa.eu/eli/reg_impl/2025/1234/oj/eng).
For manufacturers of medical devices and in-vitro diagnostics (IVDs), this amendment to Commission Implementing Regulation (EU) 2021/2226 represents an important step toward digital product documentation, while maintaining the safety principles established under the Medical Device Regulation (EU) 2017/745 and the In Vitro Diagnostic Regulation (EU) 2017/746.
eIFU Remain Limited to Professional-Use Devices
A key regulatory principle remains unchanged: electronic instructions for use may only replace paper instructions for devices intended exclusively for professional users.
Devices intended for lay users, home-use diagnostics, or consumer healthcare applications must continue to include paper instructions for use. Manufacturers must therefore carefully evaluate the intended user group and foreseeable use scenarios during regulatory classification and risk management.
Regulatory Requirements under MDR and IVDR
Both MDR and IVDR define general obligations regarding the information supplied with medical devices and IVDs.
Key provisions include:
MDR Article 10(11) and Annex I Chapter III, 23
IVDR Article 10(10) and Annex I Chapter III, 20
These sections require manufacturers to ensure that instructions for use are:
clear and understandable
accessible to the intended user
kept up to date throughout the device lifecycle.
In addition, the norm EN ISO 20417:2021 Medical devices - Information to be supplied by the manufacturer is useful as support for the preparation of the instruction for use.
A Key Advantage: Managing EU Language Requirements
One of the most practical advantages of eIFU is the simplified management of national language requirements across the EU.
Under MDR and IVDR, instructions for use must be provided in the official language(s) required by each Member State where the device is made available. (See EU overview of language requirements https://health.ec.europa.eu/publications/overview-language-requirements-manufacturers-medical-devices_en)
For manufacturers distributing devices in multiple EU markets, this often means maintaining a large number of translated IFU versions.
A compliant eIFU platform enables manufacturers to:
host all required translations in one central location
provide immediate access to the correct language version
update individual translations without reprinting entire manuals.
If all required translations are available electronically, manufacturers can more efficiently meet EU language compliance obligations while avoiding complex logistics related to multilingual printed instructions.
Operational Benefits of eIFU
Beyond language management, eIFU offer several additional advantages for Regulatory Affairs and Quality teams.
Faster safety updates
Electronic IFU allow manufacturers to publish updated instructions immediately after regulatory approval.
Improved document control
Digital platforms support version tracking, traceability, and archived access to previous IFU versions.
Sustainability and logistics efficiency
Reducing printed documentation decreases packaging volume and environmental impact.
Key Compliance Considerations
Despite these benefits, manufacturers must address several regulatory requirements.
Risk Assessment
The manufacturer must perform a documented risk assessment to show that providing IFUs electronically maintains or improves safety compared with paper.
Availability and Access
eIFUs must be available in all EU Member States where the device is placed on the market, unless justified otherwise in the risk assessment.
They must be accessible on a website or electronic medium and provided in a commonly used format that can be read with freely available software.
Website Requirements
Websites used to host eIFUs must meet the following conditions:
Protected against unauthorized access and tampering.
Stable internet address, directly accessible.
Must fulfil data protection requirements (GDPR).
Ensure minimal server downtime and display errors.
Request for Paper Version
Even if IFUs are delivered electronically, manufacturers must have a system to provide a paper version at no extra cost upon user request, normally within 7 calendar days of request.
Labeling
Manufacturers must clearly indicate on the device label or packaging that instructions are supplied electronically and provide information on how to access them.
Retention and Versions
eIFUs must be retained in electronic form for specified periods after the device is last placed on the market:
10 years for devices with a defined expiry date (except implantable).
15 years for implantable devices or devices without a defined expiry date.
Historical versions (including publication dates) must be accessible on the website or, if obsolete, available on request.
Connection to UDI and Eudamed
Once Eudamed’s UDI database registration becomes mandatory, the manufacturer must provide the internet address (URL) where the eIFU is accessible to the database.
Conclusion
The updated EU eIFU framework expands opportunities for digital instructions for use across the medical device sector. However, manufacturers must ensure strict compliance with regulatory conditions—particularly the requirement that eIFU replacing paper instructions are only permitted for devices intended exclusively for professional users.
When implemented correctly, eIFU not only support regulatory compliance under MDR and IVDR but also provide a significant advantage in managing multilingual documentation across the European market.

Regulatory Updates

EU Expands eIFU Eligibility: Key Changes under Implementing Regulation (EU) 2025/1234

The EU expands the use of electronic Instructions for Use (eIFU) for professional-use medical devices under Implementing Regulation (EU) 2025/1234. Key compliance considerations for MDR and IVDR manufacturers.

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The European Commission has adopted Commission Implementing Regulation (EU) 2026/977, introducing binding uniform rules on how notified bodies must handle quotations, conformity assessment timelines, and re-certification. For manufacturers of medical devices and in vitro diagnostic (IVD) medical devices, this regulation brings long-awaited predictability - and specific new compliance obligations.

Regulatory Updates

EU Regulation 2026/977: What Medical Device Manufacturers Need to Know About New Notified Body Rules

The European Commission has adopted Commission Implementing Regulation (EU) 2026/977, introducing binding uniform rules on how notified bodies must handle quotations, conformity assessment timelines, and re-certification. For manufacturers of medical devices and in vitro diagnostic (IVD) medical devices, this regulation brings long-awaited predictability - and specific new compliance obligations.

MedNet EC-REP06. Mai 2026

Regulatory Updates

MDCG 2025-10: New PMS Guidance for MDR & IVDR

The MDCG released new PMS guidance in December 2025. Learn what MDCG 2025-10 means for your MDR and IVDR compliance strategy.

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New swissdamed registration fees - what manufacturers need to know from 2027

Background: the swissdamed database

The new fee structure from 2027

Who pays - and when?

What this means for your swissdamed registration

How MedNet supports you

Related Articles

EU Expands eIFU Eligibility: Key Changes under Implementing Regulation (EU) 2025/1234

EU Regulation 2026/977: What Medical Device Manufacturers Need to Know About New Notified Body Rules

MDCG 2025-10: New PMS Guidance for MDR & IVDR

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