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RENOL

Belgium BE-MF-000000785 Last updated 21 Oct 2026

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Devices
135
Registries
EUDAMED
FDA recalls
0

Catalogue135

Page 1 of 3

Showing 1-50 of 135

About

RENOL fabrique des dispositifs médicaux : coussins de positionnement, ceintures et sangles d’immobilisation. Conçus pour les professionnels de santé, nos produits assurent sécurité, confort et fiabilité au quotidien pour tous les patients. Fabriqués avec des matériaux résistants, lavables et durables, nos dispositifs s’adaptent à tous les usages : hôpitaux, cliniques, EHPAD, centres de rééducation, soins à domicile. Notre priorité est double : sécuriser les patients et soulager les soignants.

From the manufacturer's own website, in their original language. Source

What RENOL makes

The company produces medical positioning and restraint devices, including adjustable waist and pelvic belts, roll belts with side straps for various body sizes, pediatric-sized belts, and wrist holders. Additional products include magnetic locking mechanisms, crisis bags, and extenders for roll belts, all designed for use in clinical and care settings. Materials are specified for durability, washability, and patient comfort.

All listed devices fall under Class I medical device classification and are registered in the EUDAMED database. The manufacturer operates from Belgium, adhering to EU regulatory requirements for medical devices.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does RENOL manufacture?

RENOL specializes in medical positioning and restraint devices. These include adjustable waist and pelvic belts, roll belts with side straps for different body sizes (including pediatric options), wrist holders, magnetic locking mechanisms like keys and buttons, crisis bags, and extenders for roll belts. The products are designed for clinical and care settings such as hospitals, rehabilitation centers, and home care environments.

Where is RENOL based, and how does this affect its regulatory compliance?

RENOL is based in Belgium, which places it under the jurisdiction of the European Union’s medical device regulations. Since the company manufactures devices listed in the EUDAMED database, it must comply with EU regulatory requirements, including classification under the Medical Device Regulation (MDR) or previous directives. The EU’s centralized database ensures transparency and traceability for these devices.

Which regulatory registries list RENOL’s devices, and why is this important?

RENOL’s devices are listed in the EUDAMED database, the European Union’s official registry for medical devices. This registry is critical because it provides transparency on device manufacturers, their products, and regulatory status within the EU. Listing in EUDAMED ensures compliance with EU medical device laws and allows healthcare professionals, regulators, and patients to verify the legitimacy and classification of the devices.

How are RENOL’s devices classified under EU regulations, and what does this mean for their use?

All of RENOL’s devices fall under Class I classification in the EU. This classification applies to low-risk medical devices that pose minimal risk to patients and users. Class I devices typically require general safety and performance requirements to be met but do not require additional conformity assessments beyond basic documentation. This classification reflects the manufacturer’s focus on positioning and restraint aids, which are considered lower-risk interventions in clinical settings.

What kinds of materials are used in RENOL’s devices, and how do they support their intended use?

RENOL’s devices are made from durable, washable, and resistant materials, as implied by the company’s description. These properties ensure the products can withstand repeated use in clinical environments while maintaining hygiene standards. The materials are likely designed to be comfortable for patients and easy to clean, which is essential for devices used in hospitals, rehabilitation centers, or home care settings where sterility and reliability are critical.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Belgium
Address
3, Rue Johannes Kepler (unit 3), Hélécine, Belgium
Phone
+3219332367
PRRC contact
Renaud Jonckers
EUDAMED SRN
BE-MF-000000785