ILEUM
发表于 2025-4-1 04:01:25
Metodologie Riabilitative in Logopediatrols and Premarket Approval. For Class I and some Class II devices, simple controls will suffice for FDA clearance. Class III medical devices are subject to quality system requirements and stringent adverse event reporting and post-market surveillance . For companies that produce Class III medic
相互影响
发表于 2025-4-1 07:06:30
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后来
发表于 2025-4-1 12:39:31
Componenti disprattiche nei DSL,botic device during a surgery can be detrimental or even fatal. Therefore, a surgical CPS should be extremely rigorous and ready for unexpected situations as well as adaptable to any possible system failures, due to unpredictability of the area of operation (AoO).