§ COMPARE REGULATORS

CDSCO vs COFEPRIS: Medical Device Regulatory Comparison

Compare the medical device registration pathways, classification, and regulatory requirements of CDSCO (India) vs COFEPRIS (Mexico).

CDSCO

Central Drugs Standard Control Organization (India)

India

India's CDSCO regulates medical devices under the Medical Devices Rules 2017 (amended 2020). India uses a four-class system (A, B, C, D). India is the fastest-growing major medical device market globa

CLASSES

Class A, B, C, D

PATHWAY

CDSCO registration / import license

KEY FUNCTIONS
  • Medical device registration
  • Import license (Form MD-14)
  • Clinical investigation approval
  • Quality management system audit
  • Adverse event reporting

COFEPRIS

Federal Commission for Protection against Health Risks (Mexico)

Mexico

COFEPRIS regulates medical devices in Mexico under the General Health Law. Mexico uses a three-class system (I, II, III). A sanitary registration (registro sanitario) is required for Class II and III

CLASSES

Class I, II, III

PATHWAY

COFEPRIS sanitary registration

KEY FUNCTIONS
  • Sanitary registration
  • FDA/EU recognition pathway
  • GMP compliance
  • Import permits
  • Vigilance reporting

MedFlux monitors both CDSCO and COFEPRIS in real time — every regulatory change, safety alert, and market signal delivered in under 90 seconds.

COMPARE LIVE DATA FREE →

§ OTHER COMPARISONS