IVD Classification
What is an IVD?
An in vitro diagnostic (IVD) medical device is any device — including reagents, kits, instruments, and software — intended to examine specimens derived from the human body, such as blood, urine, tissue, or swabs, to provide information for diagnosis, monitoring, or prognosis.
IVDs notified under Schedule II of MDR 2017 are subject to CDSCO licensing.
IVD risk classification
IVDs follow a distinct classification track based on two axes:
- Risk to the individual patient (personal health consequence of incorrect result);
- Risk to public health (impact of widespread incorrect results, e.g., for communicable disease screening).
| Class | Risk profile | Examples |
|---|---|---|
| Class A | Low individual / low public health | General chemistry reagents, blood cell counters |
| Class B | Moderate individual / low public health | Pregnancy tests, fertility hormones, PSA kits |
| Class C | High individual / moderate public health | Blood glucose meters, blood gas analysers, HbA1c |
| Class D | High individual / high public health | HIV, Hepatitis B/C, blood group typing, COVID-19 |
Regulatory pathway for IVDs
Class A IVDs: Form MD-15 (registration). Class B, C, D IVDs: Form MD-14 (full import licence via CDSCO / SUGAM).
Performance data (analytical and clinical) from CDSCO-notified or internationally accredited laboratories is required for Class C and D IVDs.