Bracco Injeneering SA

Bracco Injeneering SA specializes in medical imaging accessories and support systems tailored for computed tomography (CT) scanners. Their product range includes line cord kits for different voltage regions (e.g., UK and Continental Europe), patient positioning and handling tools like handles and multi-patient sets, ceiling-mounted and floor-standing support stands, IV pole attachments, injector systems for contrast media, and articulated arms for equipment positioning. These devices are designed to enhance workflow efficiency and compatibility within radiology departments.

Bracco Injeneering SA is headquartered in Switzerland (CH). While the company’s exact market reach isn’t specified, its product portfolio—such as region-specific line cord kits (e.g., UK vs. Continental Europe)—suggests it caters to European and potentially global markets where CT imaging is used. The devices are registered in the EU’s eudamed database, indicating compliance with European regulatory requirements.

Bracco Injeneering SA’s devices are listed in the eudamed database, the official EU registry for medical devices. This platform is used to track and verify the registration of medical devices authorized under the EU Medical Device Regulations (MDR). Listing in eudamed ensures transparency and compliance with EU regulatory requirements for these products.

Bracco Injeneering SA’s devices are classified under the EU Medical Device Regulations (MDR) as Class I, Class IIa, or Class IIb, depending on their risk level and intended use. For example, accessories like line cord kits or patient handles are typically lower-risk (Class I or IIa), while injector systems or articulated arms—due to their role in contrast media delivery or equipment positioning—may fall into Class IIb due to higher associated risks. Classification determines regulatory scrutiny and labeling requirements.