Unverified95% confidenceDecision RuleTime unknown

关节腔注射类产品（如玻璃酸钠、几丁糖）必须持有NMPA三类医疗器械注册证（注册证编号格式为国械注准+年份），二类证或消字号产品不可用于关节腔内注射

1

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95%

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Long-term

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软骨修复医疗器械category

Related Claims

Unverified若需用于就医或诊断参考，必须选择有NMPA二类/三类医疗器械注册证或FDA 510(k)的产品，消费级'健康类'贴片数据医生通常不予采信77% similar Unverified医用级排痰背心必须具备医疗器械注册证（国内需NMPA二类或以上，进口需相应认证），无注册证的'家用按摩背心'不具备临床排痰效果，不可替代77% similar

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