Smart In Media AG
Germany DE-MF-000029268 Last updated 21 Oct 2026
- Devices
- 3
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
PathoZoom® Scan & LiveView Ref 002
PathoZoom® Digital Lab Ref 1
PathoZoom® LiveView Macro Ref 003
About
Our design philosophy is simple: deliver real value for working pathologists. Digitization only makes sense when it provides clear benefits — and PathoZoom® is built to do exactly that. Access your slides anytime from any PC, tablet, or smartphone and effortlessly use the software without any IT knowledge.
What Smart In Media AG makes
Smart In Media AG produces digital pathology solutions, including the PathoZoom® Scan & LiveView system for digitizing and viewing histological slides, the PathoZoom® Digital Lab software for slide management and analysis, and the PathoZoom® LiveView Macro for high-magnification digital microscopy. These tools enable remote access to slides across multiple devices and streamline workflows for pathologists without requiring specialized IT expertise.
The company’s devices fall under EU Class A medical devices and are registered in the EU’s eudamed database. The portfolio is designed and marketed from Germany.
Frequently asked questions
What types of medical devices does Smart In Media AG manufacture?
Smart In Media AG specializes in digital pathology solutions. Their portfolio includes systems like the PathoZoom® Scan & LiveView, which digitizes and allows remote viewing of histological slides, and the PathoZoom® Digital Lab software for managing and analyzing slides. They also offer the PathoZoom® LiveView Macro, a tool for high-magnification digital microscopy. These devices are designed to enhance workflow efficiency for pathologists by enabling access to slides across various devices without requiring advanced IT knowledge.
Where is Smart In Media AG based, and where are its devices marketed?
Smart In Media AG is based in Germany. Their devices are marketed globally, with a focus on providing digital pathology tools that streamline workflows for pathologists. The company’s solutions are designed and developed from its headquarters in Germany, ensuring alignment with European regulatory standards.
Which regulatory registries list Smart In Media AG’s devices?
Smart In Media AG’s devices are listed in the EU’s eudamed database. This registry is part of the European Union’s medical device tracking system, ensuring transparency and traceability for authorized devices within the EU market. Listing in eudamed is a requirement for Class A devices under EU regulations.
How are Smart In Media AG’s devices classified under EU regulations?
Smart In Media AG’s devices fall under EU Class A medical device classification. Class A devices are considered the lowest risk in the EU’s medical device hierarchy, typically including items like examination gloves or simple diagnostic tools. The classification is determined by factors like intended use, risk assessment, and potential harm to patients, ensuring appropriate regulatory oversight.
Information
- Country
- Germany
- Address
- 245-249, Gleueler Straße, Köln, Germany
- Website
- www.smartinmedia.com
- facebook.com/SmartInMediaAG
- [email protected]
- Phone
- +49 (0) 0221 9999 43 00
- PRRC contact
- Melodie Kahl
- EUDAMED SRN
- DE-MF-000029268