The MD-42 Trade License: Selling Medical Devices in India
Yudhisthir Joshi
Director
Who Needs an MD-42 License?
Any entity intending to sell, stock, exhibit, or distribute medical devices by wholesale in India must obtain a Registration Certificate in Form MD-42 from the State Licensing Authority (SLA). This rule applies universally, regardless of whether the devices are imported or manufactured domestically.
Key Compliance Requirements
Applying for an MD-42 license requires a specific set of documentation demonstrating the competence and infrastructure of the trading entity:
- Competent Person: You must appoint a competent technical person who holds a degree from a recognized university and has at least one year of experience in dealing with medical devices.
- Storage Infrastructure: Proof of adequate storage facilities, particularly if handling temperature-sensitive devices (e.g., IVD reagents).
- Traceability: Maintaining meticulous records of purchase and sale to ensure batch-level traceability in the event of a recall.
Without an MD-42 license, your distribution network in India is operating illegally and risks immediate seizure of goods.
Need Advisory Support?
Consult our experts to audit your Device Master File (DMF), QMS, or prepare submissions for CDSCO, EU MDR, and FDA clearances.
Request consultationRegulatory Alerts
Subscribe to receive immediate notification of global regulation modifications, SUGAM portal changes, and FDA guidelines.
Related Publications

Navigating the New CDSCO Medical Device Regulations: A Definitive Compliance Guide
Understand the regulatory shift under India's Medical Device Rules (MDR) 2017, classification pathways, and MD-15 import licensing requirements for global manufacturers.

Demystifying EU MDR Compliance: Key Steps for CE Marking in 2026
A practical guide to transitioning to the EU Medical Device Regulation (2017/745), managing Notified Body backlogs, and updating clinical evaluations.