Product group Physical therapy - massage / mobility devices
Reference 22888/25

Product group Optics / Precision engineering - endoscopes
Reference 23726/25

Product group In-vitro diagnostics - immunological products
Reference 27353/25

New guidelines have been added

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 22788/25

Product group ophthalmological technology - contact lenses
Reference 26223/25

Product group Medical data processing (software) - Facette_Produktgruppe_09md-07
Reference 27257/25

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 27308/25

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 24215/25

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 24423/25

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 25741/25

The BfArM launches a new version of the DMIDS module "Clinical investigations and performance studies" on July 1, 2025.

ICD-10-GM is a version of ICD-10-WHO adapted to the specific requirements of the German health care system and is continuously developed. The Alphabetical Index to ICD-10-GM has developed from the ICD diagnostic thesaurus of the Central Research Institute of Ambulatory Health Care in Germany (Zi). It is adapted according to the changes to the Tabular List.

OPS is an adaptation of the English-language International Classification of Procedures in Medicine (ICPM) by WHO. The German version of the ICPM resulted from the translation and expansion of the Dutch version ICPM-DE (Dutch Extension) and was further developed into OPS-301 and then OPS. The OPS is currently updated annually. The alphabetical index is updated according to changes in the classification system.

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 22277/25

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 36336/24

Product group Active implantable medical devices - defibrillators
Reference 26815/25

Product group Medical instruments for use in humans - visceral surgery
Reference 23237/25

Active substance: odium oxybate The European Medicines Agency (EMA) is starting to review medicines containing sodium oxybate.

Effective July 1, 2025, new regulations will apply to radiation protection approvals or notifications for clinical trials.