Meyra GmbH
Fabricante alemán de sillas de ruedas manuales y eléctricas, venta al por mayor de rehabilitación.
Meyra fabrica sillas de ruedas, scooters y equipos de rehabilitación en su planta de Kalletal en Renania del Norte-Westfalia desde 1936. La gama abarca sillas de operador manuales, sillas de ruedas activas autopropulsadas y modelos eléctricos para interiores y exteriores. La distribución se realiza a través de mayoristas de dispositivos médicos y especialistas en rehabilitación en toda Alemania y Europa Central.
- Type
- brand seeking distribution
- Location
- Kalletal, Germany
- Founded
- 1936
- Website
- meyra.com
- Categories
- Suministros médicos y sanitarios
- Markets
- Alemania, Austria, Polonia, Países Bajos, Francia
Verified facts
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- domain-registered (green), checked 2026-08-02 Domain registry record
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
- registry-active-global (green), checked 2026-08-17 Marktstammdatenregister (Bundesnetzagentur)
- registered-since (green), checked 2022-11-29 Marktstammdatenregister (Bundesnetzagentur)
- vat-valid (green), checked 2026-08-13 VIES (European Commission)
Profiles
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- AEO, Authorised Economic Operator EU AEO database
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)