Our offers

Solutions by role

QARA & regulatory affairsbuild your profile page
Manufacturersenrich your page for free

Features & tools

HTTP APIto embed the medical-device market in your tools
DataVizspot the trends at a glance
MCP serverThe medical-device market, inside your AI assistant
Monitoring & alertsof MedTech companies
Data exportsof your search results
Data enrichmentof all your company dataContact us
CRMto enrich your recordsContact us
DataMatrix generationcompliant DataMatrix generation
UDI scanningidentify medical devices by scanning them
Compliance supportsupport for your regulatory needsContact us
Commercial intelligencespot commercial opportunitiesContact us
Company mappingthe relationship graph of companiesContact us
Featured placementat the top of search results

PricingAll featuresContact us

Pricing Sign in

© 2026 Made In Tracker

Explore

Companies Devices Documents Persons

Resources

Blog FAQ Glossary About Features

Company

Pricing Partners Refer & earn Top referrers Contact

Legal

Privacy Policy Legal Notice

Ecosystem

Made In Tracker (opens in new tab)EasyUDI (opens in new tab)

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Monthly EUDAMED change digest

Get a monthly digest of the new devices, certificates and manufacturers added to EUDAMED — straight to your inbox.

By subscribing, you accept the General Personal Data Protection Policy.Check the consent box to subscribe.

MDCG 2023-2 — List of Standard Fees

MD Atlas
Documents

Regulatory guidance

MDCG 2023-2

List of Standard Fees

Published Jan 1, 2023

EN

Reference

MDCG 2023-2

Source

MDCG

Topic

Notified bodies

Published

Jan 1, 2023

Languages

EN

Official document

Open document (PDF)View on the official source

© European Union — European Commission, DG SANTE. Reuse under CC BY 4.0.

Related documents

MDCG 2019-6
Questions and answers: Requirements relating to notified bodies
Published Feb 1, 2025
MDCG 2021-15
Application form to be submitted by a conformity assessment body when applying for designation as notified body under the medical devices regulation (MDR)
Published Jan 1, 2025
MDCG 2021-15/MDCG 2024-7 Annex
Annex to Application Form & PAR Template MDR (List of documents)
Published Jan 1, 2025
MDCG 2021-16
Application form to be submitted by a conformity assessment body when applying for designation as notified body under the in vitro diagnostic devices regulation (IVDR)
Published Jan 1, 2025