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meda
BillingFinds the codes your PVS misses
EBMStatutory billing (GKV) GOÄPrivate billing HzVGP-centred care contracts
NotesClean documentation in seconds
IntegrationsWorks with any practice software (PVS)
By organization
PracticesLess paperwork, fewer missed codes MVZ & multi-siteOne standard across every site, with oversight Practice networksOne standard for every member practice, each stays independent Billing officesEvidence-backed codes from the practice, before they reach you
By role
Doctormeda writes the note, you approve every code Biller & nurses (MFA)A daily list of missed codes, each with its evidence ManagementRuns the whole organization on numbers, not guesswork
Pricing Security
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Product
BillingFinds the codes your PVS misses
EBMStatutory billing (GKV) GOÄPrivate billing HzVGP-centred care contracts
NotesClean documentation in seconds IntegrationsWorks with any practice software (PVS)
Who we serve

By organization

PracticesLess paperwork, fewer missed codes MVZ & multi-siteOne standard across every site, with oversight Practice networksOne standard for every member practice, each stays independent Billing officesEvidence-backed codes from the practice, before they reach you

By role

Doctormeda writes the note, you approve every code Biller & nurses (MFA)A daily list of missed codes, each with its evidence ManagementRuns the whole organization on numbers, not guesswork
Pricing Security
Company
About Insights Careers
Log in Deutsch
Try for free Talk to us

Legal

RegulatoryRegulatorik

How meda is classified under the MDR and the AI Act. For practice IT, data protection officers and management.

01Intended purpose

meda produces structured documentation from the consultation and proposes billing codes under EBM, GOÄ and HzV, each with the supporting passage. The physician decides, and nothing enters your practice management system (PVS) without their release.

02Not a medical device

meda is not a medical device within Regulation (EU) 2017/745. meda makes no diagnosis and gives no treatment recommendation. Our classification assessment is available on request.

03AI Act

meda is not a high-risk AI system under Regulation (EU) 2024/1689. meda is the provider, your practice the deployer. Training material on AI literacy (Art. 4) for your team is available on request.

Questions: support@mymeda.ai · Last updated: 07.10.2026

Wie meda nach MDR und KI-Verordnung eingestuft ist. Für Praxis-IT, Datenschutzbeauftragte und Geschäftsführungen.

01Zweckbestimmung

meda erstellt aus dem Gespräch eine strukturierte Dokumentation und schlägt Abrechnungsziffern nach EBM, GOÄ und HzV vor, jede mit der stützenden Stelle. Die Entscheidung trifft die Ärztin oder der Arzt, und nichts geht ohne ärztliche Freigabe in Ihr Praxisverwaltungssystem (PVS).

02Kein Medizinprodukt

meda ist kein Medizinprodukt im Sinne der Verordnung (EU) 2017/745. meda stellt keine Diagnose und gibt keine Behandlungsempfehlung. Unsere Einstufungsbewertung erhalten Sie auf Anfrage.

03KI-Verordnung

meda ist kein Hochrisiko-KI-System im Sinne der Verordnung (EU) 2024/1689. meda ist Anbieter, Ihre Praxis Betreiber. Schulungsunterlagen zur KI-Kompetenz (Art. 4) für Ihr Team erhalten Sie auf Anfrage.

Fragen: support@mymeda.ai · Stand: 07.10.2026

meda

The billing-completeness layer above the PVS. For German ambulant care. Built in Munich.

Product

Billing Reads EBM · GOÄ · HzV Notes Integrations Pricing

Who we serve

Practices MVZ & multi-site Practice networks Billing offices

Company

About Insights Careers Book a demo

Trust

Security Der meda Kodex Data Processing Agreement (AVV) Regulatory
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