§ COMPARE REGULATORS

PMDA vs HSA: Medical Device Regulatory Comparison

Compare the medical device registration pathways, classification, and regulatory requirements of PMDA (Japan) vs HSA (Singapore).

PMDA

Pharmaceuticals and Medical Devices Agency (Japan)

Japan

Japan's PMDA conducts scientific reviews of medical device applications under the PMD Act. Japan uses a four-class system with three pathways: Todokede (notification) for Class I, Ninsho (third-party

CLASSES

Class I, II, III, IV

PATHWAY

Todokede / Ninsho / Shonin

KEY FUNCTIONS
  • Shonin pre-market approval
  • Ninsho third-party certification
  • QMS inspection (MHLW Ordinance 169)
  • PMDA consultation (Taimen Joshu)
  • Foreign Manufacturer Registration

HSA

Health Sciences Authority (Singapore)

Singapore

Singapore's HSA regulates medical devices using a four-class risk-based system (A, B, C, D). HSA accepts conformity assessment from recognized bodies and is a founding member of IMDRF. Singapore serve

CLASSES

Class A, B, C, D

PATHWAY

HSA registration

KEY FUNCTIONS
  • Device registration (Class B-D)
  • Class A dealer license
  • GN-13 guidance compliance
  • Adverse event reporting
  • IMDRF participation

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§ OTHER COMPARISONS