assist GmbH

Medical Technology · Merzig-Wadern

assist GmbH is a medical technology company based in Merzig-Wadern, Germany. The company operates in the German medical devices market under the EU Medical Device Regulation (MDR 2017/745).

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assist GmbH – Address & Contact

Address

In der Bruchwies 10
66663 Merzig-Wadern

assist GmbH Overview

assist GmbH is a medical technology company based in Merzig-Wadern, Saarland. The company develops, produces or distributes medical devices, instruments or systems for use in healthcare facilities.

Products & Solutions

As a medical technology company, assist GmbH offers solutions for medical facilities, clinics and practices. All products must meet the requirements of the EU Medical Device Regulation (MDR 2017/745) and bear the CE mark.

Location & Contact

assist GmbH can be reached at the following address: Bruchwies 10, 66663 Merzig-Wadern. For current information and inquiries, please contact the company directly.

More information: Medizintechnik in Saarland or all Medizintechnik in Germany on Sanoliste.

Medizinprodukte-Regulierung (MDR)

Since May 2021, medical technology companies like assist GmbH have had to comply with the EU Medical Devices Regulation (MDR 2017/745), which sets significantly stricter requirements for clinical assessments, traceability and post-market surveillance than the previous directive. All medical devices require CE marking by a notified body and must be registered in the European database EUDAMED.

Branche & Marktumfeld

The German medical technology industry is one of the most innovative industries with over 250,000 employees and a turnover of around 38 billion euros. assist GmbH in Merzig-Wadern is part of this ecosystem. Germany is the third largest medical technology market in the world after the USA and China. Over 90 percent of the approximately 1,500 medical technology companies are small and medium-sized companies (SMEs), which are often leaders in specialized niches.

Qualitätsmanagement & Zertifizierung

A quality management system in accordance with ISO 13485 is standard practice in the industry for the production and sale of medical devices. The standard defines requirements for the development, production, installation and maintenance of medical devices. In addition, the MDR requires extensive technical documentation, clinical assessments and systematic risk management according to ISO 14971 over the entire product life cycle.

Frequently asked questions about assist GmbH

What does assist GmbH do?

assist GmbH is a company in the medical technology sector based in Merzig-Wadern. The company develops, manufactures or distributes medical devices, instruments or systems for use in healthcare facilities.

Where is assist GmbH based?

assist GmbH is based in Merzig-Wadern. Detailed information can be found on the company website.

In which area of medical technology does assist GmbH operate?

assist GmbH operates in the medical technology sector and offers solutions for healthcare facilities, hospitals and practices. The exact areas of activity can be found on the company website.

What is the EU Medical Device Regulation (MDR)?

Die MDR (Medical Device Regulation, EU 2017/745) ist seit Mai 2021 die maßgebliche Verordnung für Medizinprodukte in der EU. Sie ersetzt die frühere Richtlinie 93/42/EWG und stellt strengere Anforderungen an klinische Bewertungen, Post-Market-Surveillance und Rückverfolgbarkeit. Unternehmen wie assist GmbH müssen die MDR-Konformität für alle Produkte nachweisen.

What does the CE marking mean for medical devices?

The CE marking confirms that a medical device meets the requirements of the EU Medical Device Regulation. For products in risk classes Is, Im, Ir, IIa, IIb and III, the involvement of a Notified Body is required to carry out the conformity assessment.

What risk classes exist for medical devices?

Medizinprodukte werden in vier Risikoklassen eingeteilt: Klasse I (geringes Risiko, z.B. Verbandmaterial), Klasse IIa (mittleres Risiko, z.B. Hörgeräte), Klasse IIb (erhöhtes Risiko, z.B. Infusionspumpen) und Klasse III (hohes Risiko, z.B. Herzschrittmacher). Die Klassifizierung bestimmt den Umfang der Konformitätsbewertung.

assist GmbH on social media

Medical Technology in Saarland

All Medical Technology in Saarland on Sanoliste — or discover all categories by federal state.

Last updated: 20.03.2026 · Category: Medical Technology