MIXED.Industries B.V.

MIXED.Industries B.V. specializes in mobility aids and personal care devices. Their product range includes items like arm slings, rollators (in various colors), grab rails, walking canes, elbow crutches, urinals for men and women, bed rope ladders, and toilet seat risers with lids. These devices are designed to assist with daily activities and mobility, falling under the category of Class I medical devices.

MIXED.Industries B.V. is headquartered in the Netherlands. Since its devices are classified as EU Class I medical devices, they must comply with EU Medical Device Regulations. The company’s products are listed in the EUDAMED database, which is the official EU registry for medical devices, ensuring transparency and traceability of their regulatory status.

MIXED.Industries B.V.’s devices are registered in the EUDAMED database, the European Union’s central registry for medical devices. This registry is critical because it provides official documentation of device compliance, manufacturer details, and regulatory information. For healthcare providers, distributors, or regulators, checking EUDAMED confirms that the devices meet EU requirements and are legally placed on the market.

All of MIXED.Industries B.V.’s devices fall under EU Class I classification. This means they pose the lowest risk among medical devices and typically require only general safety and performance requirements to be met, such as good manufacturing practices (GMP) and conformity assessments. Class I devices still must comply with EU regulations but generally undergo less stringent scrutiny than higher-risk classes.

Yes, MIXED.Industries B.V. markets its devices under its own VITILITY brand but also provides private-label options for B2B customers. Regardless of branding, all devices—whether sold under VITILITY or another label—must still comply with EU medical device regulations and be listed in EUDAMED under the manufacturer’s details. The registry reflects the device’s regulatory status, not its branding.