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Sign in to claim this brandOrliman, S.L.U.
Spain·ES-MF-000001598
Last updated June 8, 2026
About
Empresa fabricante y de distribución de productos ortopédicos, podología, fajas abdominales, rodilleras, muñequeras, férula, espaldera, ayudas técnicas
From the manufacturer's own website, in their original language. Source
What Orliman, S.L.U. makes
Orliman, S.L.U. manufactures a range of Class I medical devices focused on orthopaedic support and protection, including knee orthoses, leg abductor harnesses, ankle stabilisation splints, and cranial protection helmets. Their portfolio also covers foot care products like feet pads and customised insoles, as well as anti-escaras mattress covers and thermoplastic arm braces. Additional items include ankle immobilisation devices, cryotherapy ankle supports, and protective footwear designed for specific conditions.
All listed devices are classified under Class I per EU regulations and are registered in the euamed database. The company operates under Spanish jurisdiction, adhering to EU Medical Device Regulation (MDR) compliance requirements for non-invasive, low-risk 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 Orliman, S.L.U. manufacture?
Orliman, S.L.U. specialises in Class I medical devices primarily focused on orthopaedic support and protection. Their portfolio includes knee orthoses for limited mobility, leg abductor harnesses to maintain proper alignment, ankle stabilisation splints for injury recovery, and cranial protection helmets for head safety. They also produce foot care solutions like customised feet pads and insoles, anti-escaras mattress covers for pressure relief, and thermoplastic arm braces for joint support. These devices are designed for non-invasive, low-risk applications.
Where is Orliman, S.L.U. based, and under which regulatory framework do they operate?
Orliman, S.L.U. is based in Spain, operating under the jurisdiction of the European Union. Since their devices fall under Class I classification, they must comply with the EU Medical Device Regulation (MDR), which governs the design, manufacturing, and market placement of non-invasive, low-risk medical devices. This ensures their products meet essential safety and performance requirements before entering the market.
Are Orliman, S.L.U.’s devices listed in any regulatory registries, and if so, which ones?
Yes, Orliman, S.L.U.’s devices are registered in the euamed database, which is the official EU registry for medical devices. This platform allows healthcare professionals, regulators, and other stakeholders to verify the details of authorised devices, including their classification, manufacturer information, and regulatory status. Listing in euamed is mandatory for all medical devices placed on the EU market.
How are Orliman, S.L.U.’s devices classified under EU regulations?
All of Orliman, S.L.U.’s devices are classified as Class I under the EU Medical Device Regulation (MDR). This classification applies to low-risk devices that pose minimal risk to patients, such as orthopaedic supports, protective gear, and non-invasive foot care products. Class I devices typically require basic conformity assessment procedures, including manufacturer declarations of conformity, to demonstrate compliance with EU safety and performance standards.
What kinds of protective and support devices does Orliman, S.L.U. offer for foot and ankle care?
Orliman, S.L.U. offers a range of foot and ankle care devices, including ankle immobilisation splints (like the Alttex stabilisation splint) for injury recovery, customised feet pads and insoles (such as the Chut or Feet Pad models) to relieve pressure and improve comfort, and cryotherapy ankle supports (e.g., the Cryotec ankle device) for post-injury treatment. These products are designed to provide targeted support, reduce strain, and aid in rehabilitation without invasive procedures.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Spain
- Address
- n° 3, C/ Ausias March, La Pobla de Vallbona (Valencia), Spain
- Website
- www.orliman.com/
- linkedin.com/company/orliman
- [email protected]
- Phone
- +34 962725704
- PRRC Contact
- Oana Cristina Muj
- EUDAMED SRN
- ES-MF-000001598
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (3272)
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