GS Elektromedizinische Geräte G. Stemple GmbH was founded in 1982 by the Managing Director and proprietor Günter Stemple. The GS mission ever was (and still is) to design and engineer innovative products, rugged and suitable for preclinical cardiotherapy treatment.

The company is located in Kaufering/Bavaria. The world-wide distribution is outsourced and based on independent external companies. In its home office both development and production of the corpuls equipment is carried out.

Even in times of globalisation and cost pressure GS focuses on highly trained engineers and quality “made in Germany”.We don’t leave something to chance! Each unit is examined thoroughly before leaving our factory. Every single employee of our company stands up for that.

The essential aspect in the product philosophy is to be found in every single part the product range of GS Elektromed. Geräte G. Stemple GmbH: Highest possible quality, paired with reliability and ruggedness of each manufactured defibrillator/ patient monitoring systems in order to meet the special requirements in the Emergency Medical markets.

 Already in the design phase, GS development ensures that future corpuls hard- and software updates are easy upgradable. Without them having to purchase a new device, they may update their corpuls defibrillator and patient monitoring system to the latest state-of-the-art, at any time.
 
Imprint: http://corpuls.world/imprint?lang=en


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corpuls | GS Elektromedizinische Geräte G. Stemple GmbH

corpuls | GS Elektromedizinische Geräte G. Stemple GmbH's headquarters in Kaufering, Germany

This department focuses on designing, implementing, and maintaining software applications and embedded systems.

Software Development

The Product Management team at corpuls | GS Elektromedizinische Geräte G. Stemple GmbH is responsible for overseeing the development lifecycle of the company's cardiotherapy treatment devices, including defibrillators and patient monitoring systems. This team ensures that products meet the highest standards of quality, reliability, and ruggedness, and are designed to be easily upgradable. They work closely with engineers to oversee product design, coordinate software and hardware updates, and align the product portfolio with market needs and customer feedback.

Product Management

The Project Management team at GS Elektromedizinische Geräte G. Stemple GmbH oversees and coordinates the design and development of innovative preclinical cardiotherapy products. This team ensures projects are completed on time, within budget, and to the highest quality standards, supporting continuous improvements and upgrades in corpuls hardware and software. They collaborate closely with engineering, production, and external distribution partners to deliver reliable and rugged defibrillator and patient monitoring systems that meet the demanding requirements of the emergency medical market.

Project Management

This department focuses on providing educational resources and training related to clinical practices and standards.

Clinical Education

This department oversees compliance with regulations and guidelines to ensure product safety and efficacy.

Regulatory Affairs

This department focuses on the collection, analysis, and engineering of data to support informed decision-making.

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Product Management

Project Management

Clinical Education

Regulatory Affairs

Data Management