classify_device
RUNS WITHOUT AN API KEY (anonymous callers see the top 3 FDA product codes and the full per-market risk table — a free key unlocks the rest). Classification view of a device type: the GMDN hierarchy it sits in, the FDA product codes it maps to with how many devices carry each, and — the part not published anywhere — how the SAME device type is actually risk-classed market by market, with the sample size behind each. Risk class is not portable: a device type can be modal High in Canada and modal Medium in the EU and Singapore, which changes submission route, evidence burden and timeline. Observed practice, not a regulatory determination. Takes a plain device name ("bone screw", "hip implant"), a GMDN code, or an FDA product code. A name is resolved by how many real devices carry each GMDN term rather than by string matching, and resolution reports which term was chosen, how many others matched and what they were — call again with gmdn_code to classify one of those instead.
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| gmdn_code | No | GMDN code, e.g. "44727" | |
| device_type | No | A device name in plain words ("insulin pump", "orthopaedic plate") or a GMDN term. US and British spellings both resolve. Name the device, not the brand or the use — "infusion pump", not "PumpMaster 3000" or "for giving fluids". Where the name fits several device types, the reply says so in `resolution`. | |
| fda_product_code | No | FDA product code, e.g. "DZE" |