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类别: REGULATORY PATHWAYS

承认(日本上市前批准)

PMDA/厚生劳动省对日本II类(无标准)、III类和IV类医疗器械的上市前批准途径。承认包括PMDA科学审评和厚劳省正式批准。

Last reviewed 2026-08-05 · Reviewed by MedFlux Editorial Board · Editorial policy

Expanded process notes below are currently maintained in English; the short definition above is localized. See our editorial policy.

WHEN IT APPLIES

Shonin is Japan’s PMDA/MHLW pre-market approval path for higher-risk devices (typically Class III/IV and some Class II without standards).

PROCESS / STEPS

  1. Confirm Japanese classification and pathway (Shonin vs Ninsho vs Todokede).
  2. Engage a DMAL holder.
  3. Prepare dossier and consult PMDA as needed.
  4. Complete review and MHLW authorization; plan PMS.

EXAMPLES

  • A novel implant without a certification standard typically requires Shonin rather than Ninsho.

RELATED GUIDES & TOOLS

SOURCES

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