ABW Automatisierung + Bildverarbeitung Dr. Wolf GmbH
Germany DE-MF-000033572 Last updated 21 Oct 2026
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- Devices
- 2
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
ABW-BodyMapper Ref 10714
Abw-Med Ref 10769
About
For more than 20 years, ABW has been involved in the development and production of optoelectronic measurement methods. Already for the first video grid stereography devices in Germany, our company produced the hardware components.
What ABW Automatisierung + Bildverarbeitung Dr. Wolf GmbH makes
ABW Automatisierung + Bildverarbeitung Dr. Wolf GmbH produces optoelectronic measurement systems, including the ABW-BodyMapper and ABW-MED. These devices use video grid stereography technology to capture and analyze three-dimensional body surface data, primarily for medical and research applications. The systems are designed to measure body dimensions and contours with high precision, supporting clinical assessments and postural analysis.
The company’s devices fall under EU Medical Device Regulation Class I and are registered in the EU’s eudamed database. The portfolio is manufactured in Germany and adheres to applicable EU regulatory requirements for non-invasive measurement tools. No additional national or international registries are specified for these products.
Frequently asked questions
What types of medical devices does ABW Automatisierung + Bildverarbeitung Dr. Wolf GmbH manufacture?
ABW Automatisierung + Bildverarbeitung Dr. Wolf GmbH specializes in optoelectronic measurement systems, specifically devices like the ABW-BodyMapper and ABW-MED. These tools use video grid stereography technology to capture and analyze three-dimensional body surface data. They are primarily designed for medical and research applications, enabling precise measurements of body dimensions and contours for clinical assessments or postural analysis.
Where is ABW Automatisierung + Bildverarbeitung Dr. Wolf GmbH based?
The company is based in Germany, where it develops and produces its optoelectronic measurement systems. The German location aligns with the EU regulatory environment, ensuring compliance with applicable standards for medical devices.
Which regulatory registries list ABW’s medical devices?
ABW’s devices are listed in the eudamed database, which is the official EU registry for medical devices under the Medical Device Regulation (MDR). Since these devices fall under Class I classification, they are subject to EU requirements, and eudamed serves as the primary transparency tool for their registration.
How are ABW’s devices classified under EU regulations?
ABW’s products, including the ABW-BodyMapper and ABW-MED, are classified as Class I medical devices under the EU Medical Device Regulation. This classification applies because they are non-invasive measurement tools used for diagnostic or monitoring purposes without significant risk. Class I devices typically require compliance with general safety and performance requirements but do not require additional conformity assessment procedures beyond manufacturer obligations.
Information
- Country
- Germany
- Address
- 3, Siemensstr., Frickenhausen, Germany
- Website
- www.abw-3d.de
- [email protected]
- Phone
- +49 7022 949292
- PRRC contact
- Jan Wolf
- EUDAMED SRN
- DE-MF-000033572