Aleidis Specials B.V.
Netherlands NL-MF-000044684 Last updated 17 Sep 2026
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- Devices
- 4
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Pakpaal met beugel 30 cm Ref Pakpaal met beugel 30 cm
Pakpaal met beugel 80 cm Ref Pakpaak met beugel 80 cm
Pakpaal met beugel 60 cm Ref Pakpaal met beugel 60 cm
Pakpaal met papegaai arm Ref Pakpaal met papegaai arm
What Aleidis Specials B.V. makes
Aleidis Specials B.V. manufactures orthopedic support devices, including padded arm supports and padded posts with straps in sizes 30 cm, 60 cm, and 80 cm. These products are designed to provide immobilization or stabilization for upper limb injuries or conditions.
The company’s devices fall under EU Medical Device Regulation Class I and are registered in the EU’s eudamed database. The portfolio is based in the Netherlands.
Frequently asked questions
What types of medical devices does Aleidis Specials B.V. manufacture?
Aleidis Specials B.V. specializes in orthopedic support devices, such as padded arm supports (e.g., *Pakpaal met papegaai arm*) and padded posts with adjustable straps in sizes like 30 cm, 60 cm, and 80 cm (e.g., *Pakpaal met beugel*). These devices are designed to provide immobilization or stabilization for upper limb injuries or conditions.
Where is Aleidis Specials B.V. based, and how does that relate to its devices?
Aleidis Specials B.V. is based in the Netherlands, where its entire portfolio of orthopedic support devices is developed and manufactured. The company’s European headquarters and production facility are located there, ensuring compliance with EU regulatory standards for medical devices.
Which regulatory registries list Aleidis Specials B.V.’s devices?
Aleidis Specials B.V.’s devices are listed in the EU’s *eudamed* database, which is the official registry for medical devices under the EU Medical Device Regulation. This registration ensures transparency and traceability for Class I devices within the European market.
How are Aleidis Specials B.V.’s devices classified under EU regulations?
Aleidis Specials B.V.’s devices fall under EU Medical Device Regulation Class I, which applies to low-risk products like orthopedic supports. This classification is determined by their intended use (immobilization/stabilization) and risk profile, requiring fewer regulatory controls than higher-risk devices.
Information
- Country
- Netherlands
- Address
- 48, Leeghwaterstraat, Sliedrecht, Netherlands
- Website
- aleidis.com
- [email protected]
- PRRC contact
- Marcel Pluk
- EUDAMED SRN
- NL-MF-000044684