Medical device regulation: requirements for occupational therapists in The Netherlands who prescribe and manufacture custom-made devices.

de Jong, Iwan J; Lexis, Monique A S; Slegers, Karin; Tuijthof, Gabrielle J M

de Jong, Iwan J; Lexis, Monique A S; Slegers, Karin; Tuijthof, Gabrielle J M.

Afiliação

de Jong IJ; Research Engineering, Maastricht University, Maastricht, The Netherlands.
Lexis MAS; Research Centre Assistive Technology in Care, Zuyd University of Applied Sciences, Heerlen, The Netherlands.
Slegers K; Research Centre Assistive Technology in Care, Zuyd University of Applied Sciences, Heerlen, The Netherlands.
Tuijthof GJM; Research Engineering, Maastricht University, Maastricht, The Netherlands.

Disabil Rehabil Assist Technol ; : 1-9, 2023 Mar 10.

Article em En | MEDLINE | ID: mdl-36897133

Palavras-chave

Medical Device Regulation (MDR); assistive technology; custom-made medical devices; implementation; rehabilitation; roadmap

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Disabil Rehabil Assist Technol Assunto da revista: REABILITACAO Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Holanda

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