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Medfins International > Services
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Medical Device Single Audit Program (MDSAP)

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Indian Authorised Agent

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Class A non-sterile non-measuring medical devices registration in India

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Post Submission Requests of medical device licensing in India

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Class C and D notified medical device manufacturing registration in India.

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Class C and D Medical Device Import Registration

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Class C and D notified medical device manufacturing registration in India

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MDSAP

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US FDA 510(k) Submission

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CE Marking

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OUR SERVICES

  • ISO 13485
  • CDSCO Manufacturing licence
  • CDSCO Import Licence
  • CDSCO Testing Licence
  • Indian Authorised Agent
  • Wholesale Licence
  • CE Marking
  • US FDA 510(k) Submission
  • MDSAP
  • BIS license – ISI Marking

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