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PMDA official form sinsa176

Foreign-manufactured medical-device and IVD approval succession — official blank form
JapanMinistry of Health, Labour and WelfareRegistrationCurrentness under review
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Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.

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Foreign-manufactured medical-device and IVD approval succession — official blank form is published by Ministry of Health, Labour and Welfare. This document is identified by its title; no separate official document code is recorded.

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PMDA official form sinsa176
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Japanese
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1 language version
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About this regulation

Foreign-manufactured medical-device and IVD approval succession — official blank form

Complete 2-page blank official form, including its original table layout and notes, preserved as one exact PDF expression. The captured PMDA form index links this exact URL. No printed issue or commencement date has been established. A blank form does not itself establish the legal classification, current requirements, timing or approval of a particular corporate, product-name or model change. Any other product categories printed in the form remain source context; no drug-specific rule is extended to medical devices or IVD. Present-day legal currentness remains unverified. Complete original page images govern; native extraction is a qualified, potentially incomplete search layer. No whole-country completeness or completed-question claim.

This document is identified by its title; no separate official document code is recorded. Always confirm the current consolidated text and transition provisions with the official source before filing.