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eDok – Fertigung

Creates standards-compliant technical documentation, MDR documentation, translations and UX writing with a focus on medical technology.

eDok Logo

Eisenrieth Dokumentations GmbH

Munich (Aidenbachstraße 52)New on Amplifa

1990Founded (GbR), GmbH since 1995
1995Converted to a GmbH, based in Munich
MunichCompany headquarters (HRB 118612, AG Munich)

About eDok

Eisenrieth Dokumentations GmbH (eDok) is a technical documentation service provider based in Munich. The company creates target-group-oriented and legally compliant product documentation such as instructions for use, software, operating, installation and service manuals, especially for companies in the medical technology sector. A key focus is MDR-compliant documentation for medical devices, including standards-based reprocessing instructions according to ISO 17664 and warning systems according to ISO 14971 and IEC 62366-1. Further core services are localization management and translations for medical devices in all EU languages, terminology management with the in-house system flashterm, UX writing, as well as consulting, implementation and training for editorial systems such as SCHEMA ST4. The team comprises technical editors, translation and localization experts, graphics, DTP and project management. As of October 1, 2026, kothes GmbH will acquire the business shares; eDok will remain part of the kothes group as an independent company.

Site
Munich
Processes
Technical documentation / technical editing (instructions for use, software manuals,, MDR-compliant documentation for medical devices, Localization management / translations (among others Trados Studio), UX writing for software interfaces, Implementation of an editorial system (consulting, implementation, training), Terminology management (flashterm), Creation of cleaning & reprocessing instructions according to ISO 17664 & MDR, Creation of standards-compliant warning systems according to ISO 14971 & IEC 62366-1
Materials
MDR-compliant documentation, Editorial systems (SCHEMA ST4), Terminology management, Translation Memory System, UX writing
Certificates
MDR compliance, ISO 17664 (reprocessing instructions), ISO 14971 / IEC 62366-1 (warnings)
Founded
1990 (as
Industries
Medical technology, Mechanical engineering, Consumer goods, Software
  1. 01

    Customer inquiry and needs analysis

  2. 02

    Documentation concept development

  3. 03

    Technical editing and content creation

  4. 04

    Terminology management (flashterm)

  5. 05

    Localization and translation (Trados Studio)

  6. 06

    DTP and localized graphics

  7. 07

    Review and approval

  8. 08

    Delivery in the requested file formats

Services & Tools

MDR

MDR-compliant documentation

Documentation for medical devices for safe product approval and for international markets.

SCHEMA ST4

Editorial systems (SCHEMA ST4)

Consulting, implementation, migration and training as a Quanos Silver Partner.

flashterm

Terminology management

Central maintenance of technical terms and integration into the translation memory for consistent naming.

Trados Studio

Translation Memory System

Project processing and coordination of translation and review processes.

UX-Writing

UX writing

Short, clear and consistent texts for software user interfaces.

Location

Standort Munich

Munich

DE

Company headquarters

Materials
Technical documentation, medical technology, localization
  • Trados Studio
  • flashterm
  • SCHEMA ST4
  • DTP and graphics

Service Portfolio

MDR-compliant documentation for medical devices
MDR-compliant documentation for medical devicesTechnical editing · Medical technology
Documentation of medical software
Documentation of medical softwareSoftware documentation · Medical technology
Software documentation
Software documentationTechnical editing · Software
UX writing for medical apps
UX writing for medical appsUX writing · Medical technology
Editorial system implementation (CMS/DTP)
Editorial system implementation (CMS/DTP)Consulting and training · Software

Inside the production

eDok office building in Munich
eDok office building in Munich
The eDok team
The eDok team
Employee at her workstation
Employee at her workstation
Planning day in technical editing
Planning day in technical editing
Teamwork in technical editing
Teamwork in technical editing
30th anniversary in 2025
30th anniversary in 2025
Quanos Silver Partnership certificate
Quanos Silver Partnership certificate
“MDR & Co.” – collection of regulations on medical documentation
“MDR & Co.” – collection of regulations on medical documentation

Industries

Medical technologyMechanical engineeringConsumer goodsSoftware

Processes & technical limits

ProcessesToleranceMax. partWeightLot sizeMaterials
Technical documentation / technical editing (instructions for use, software manuals,Engineering–––––
MDR-compliant documentation for medical devicesEngineering–––––
Localization management / translations (among others Trados Studio)Engineering–––––
UX writing for software interfacesEngineering–––––
Implementation of an editorial system (consulting, implementation, training)Engineering–––––
Terminology management (flashterm)Engineering–––––
Creation of cleaning & reprocessing instructions according to ISO 17664 & MDREngineering–––––
Creation of standards-compliant warning systems according to ISO 14971 & IEC 62366-1Engineering–––––

Additional services

Technical documentation / technical editingMDR-compliant documentation for medical devicesMedical technology documentationSoftware documentationEditorial system implementationLocalization managementUX writingTerminology management (flashterm)Translations for medical devicesDTP and localized graphicsTrados Studio (translation memory)SCHEMA ST4 trainingSCHEMA ST4 consulting and migration

Reference customers

FORUM (customer testimonial, exact company name not documented)

Quality & Standards Compliance

eDok complies with regulations such as the MDR, the Machinery Directive and ANSI, and creates standards-compliant reprocessing instructions according to ISO 17664 as well as warning systems according to ISO 14971 and IEC 62366-1.

EvidenceMunich
MDR compliance
ISO 17664 (reprocessing instructions)
ISO 14971 / IEC 62366-1 (warnings)

History

  1. 1990

    Started as a GbR; focus on technical documentation, in particular medical technology

  2. 1995

    Converted to Eisenrieth Dokumentations GmbH, headquartered in Munich

  3. 2025

    30th anniversary

  4. 2026

    As of October 1, kothes GmbH acquires the business shares; eDok becomes part of the kothes group

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