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一类医疗器械生产需要办许可证么
释义
法律分析:一类医疗器械不需要经营许可证。按照医疗器械风险程度,医疗器械经营实施分类管理。经营第一类医疗器械不需许可和备案,经营第二类医疗器械实行备案管理,经营第三类医疗器械实行许可管理。
法律依据:《医疗器械经营监督管理办法》 第八条 第一类医疗器械实行产品备案管理,第二类、第三类医疗器械实行产品注册管理。
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procedure for adjudication supervision
procedure for cases of private prosecution
procedure for commencement of action
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procedure for deciding on administrative penalties
procedure for enforcement
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procedure for execution of a sentence with reprieve
procedure for execution of the death sentence with a reprieve
procedure for final accounting of revenue and expenditure
procedure for handling affairs
procedure for judicial review of death sentences
procedure for modification of execution
procedure for penalties in financial administration
procedure for perpetuating testimony
procedure for reconsideration of judicial redress
procedure for rendition of judgment
procedure for renewed reconsideration
procedure for rereview
procedure for resumption of execution
procedure for signing a contract
procedure for single administrative act
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更新时间:2026/5/15 16:58:27