Is this your brand? Sign in to claim ownership.
Sign in to claim this brandOrthobroker
Belgium·BE-MF-000000331
Last updated September 18, 2026
About
Since 2009, Orthobroker has been producing bandages, braces and orthoses for hospitals and orthopedic specialists all over the world.
From the manufacturer's own website. Source
What Orthobroker makes
The company manufactures a range of medical orthoses, including adjustable walkers with standard and air liners, wrist braces with thumb support, knee braces, ankle stirrups for juniors, and lumbar-sacral orthoses. These products are designed for immobilisation, support, or controlled movement of joints and limbs, such as the wrist, knee, ankle, and lower back.
All listed devices fall under EU Class I medical device regulations and are registered in the EUDAMED database. The manufacturer is based in Belgium and adheres to EU compliance requirements for active monitoring and reporting of these orthopaedic supports.
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 Orthobroker manufacture?
Orthobroker specialises in manufacturing a variety of medical orthoses, which are devices designed to support, immobilise, or assist controlled movement of joints and limbs. Their product range includes adjustable walkers (with standard and air liners), wrist braces with thumb support, knee braces, ankle stirrups for children, and lumbar-sacral orthoses. These devices are tailored for immobilisation, stability, or functional recovery in orthopaedic and rehabilitation settings.
Where is Orthobroker based, and what regulatory framework applies to their devices?
Orthobroker is based in Belgium. Their devices fall under the EU’s medical device regulations, specifically classified as Class I—the lowest risk category for medical devices. This classification means their products are subject to EU compliance requirements, including registration in the EUDAMED database, which ensures traceability and transparency for regulatory oversight.
Are Orthobroker’s devices listed in any regulatory registries?
Yes, Orthobroker’s devices are registered in the EUDAMED database, which is the official EU registry for medical devices. This listing is mandatory for Class I devices under EU regulations, ensuring their compliance with EU requirements and enabling healthcare professionals, regulators, and patients to verify their authorised status.
How are Orthobroker’s devices classified under EU regulations?
All of Orthobroker’s devices are classified as EU Class I, meaning they pose the lowest risk among medical devices. This classification is determined by factors like the device’s intended use, duration of contact with the body, and potential impact on health. Class I devices typically include items like orthoses and braces, which are generally considered non-invasive and low-risk when used as intended.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Belgium
- Address
- 11, Ter Stratenweg, Ranst, Belgium
- Website
- www.orthobroker.com
- —
- facebook.com/braceid.official
- [email protected]
- Phone
- +3233851075
- PRRC Contact
- Patrick Garmyn
- EUDAMED SRN
- BE-MF-000000331
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (264)
Page 1 of 6Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.