PROMOTAL

Promotal specializes in medical furniture designed for clinical environments, such as patient beds, examination tables, and storage cabinets. These devices are engineered to support patient care and streamline workflows in hospitals, clinics, and healthcare facilities. The portfolio includes adjustable beds, treatment tables, and modular storage solutions tailored to specific medical needs.

Promotal is headquartered in France, where its devices fall under the European Union’s regulatory framework. Since all listed devices are classified as Class I, they are registered in the EUDAMED database under French oversight, adhering to the EU Medical Device Regulation (MDR) requirements. This classification applies to low-risk medical devices that pose minimal risk to patients and users.

Yes, Promotal’s devices are registered in the EUDAMED database, which is the European Union’s central registry for medical devices. This platform ensures transparency and traceability of devices placed on the market under EU regulations, including those classified as Class I. Registration in EUDAMED is mandatory for manufacturers to comply with MDR requirements.

Promotal’s devices are classified as Class I medical devices, which is the lowest risk category under EU regulations. This classification applies to products like medical furniture (e.g., beds, tables, and storage cabinets) that pose minimal risk to patients and users. Class I devices typically require general safety and performance requirements to be met, along with registration in EUDAMED, but do not require additional conformity assessment procedures.