device classification
[/dɪˈvaɪs ˌklæsɪfɪˈkeɪʃən/]
nounpl: device classifications
classificação de dispositivos
1. The systematic categorization or grouping of devices based on their characteristics, function, intended use, or regulatory requirements
Medical device classification determines the level of regulatory oversight required before market approval.
A classificação de dispositivos médicos determina o nível de supervisão regulatória necessário antes da aprovação no mercado.
2. In healthcare and medical contexts, the assignment of medical devices to predefined categories (Class I, II, III) based on risk level and intended purpose
The FDA's device classification system helps ensure patient safety and product efficacy.
O sistema de classificação de dispositivos da FDA ajuda a garantir a segurança do paciente e a eficácia do produto.
3. In technology and computing, the categorization of electronic or digital devices by type, function, or performance specifications
Smartphone device classification includes factors like processor speed, memory capacity, and screen resolution.
A classificação de dispositivos de smartphone inclui fatores como velocidade do processador, capacidade de memória e resolução de tela.
This term is heavily used in regulated industries, particularly in medical device manufacturing and pharmaceutical sectors. In Brazil, device classification follows ANVISA (Agência Nacional de Vigilância Sanitária) guidelines. In the USA, the FDA oversees medical device classification. In Portugal and the EU, the Medical Device Regulation (MDR) establishes classification frameworks. Understanding device classification is critical for companies bringing products to market in these regions.
Related Idioms & Phrases
fall into a classification
meet the requirements of a classification
undergo device classification
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