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Meridian Trace — Medical Device Registrations

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

TableJSON Schema
NameRequiredDescriptionDefault
gmdn_codeNoGMDN code, e.g. "44727"
device_typeNoA 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_codeNoFDA product code, e.g. "DZE"

TDQS

A4.6/5.0
Behavior5/5

Does the description disclose side effects, auth requirements, rate limits, or destructive behavior?

No annotations are present, so the description carries the full transparency burden and does it well: it discloses API-key gating, the subset of results anonymous callers see, risk-class non-portability across markets, the observed-practice caveat, and count-based name resolution. These are behavioral traits a caller could not infer from the schema alone.

Agents need to know what a tool does to the world before calling it. Descriptions should go beyond structured annotations to explain consequences.

Conciseness4/5

Is the description appropriately sized, front-loaded, and free of redundancy?

The description is long but dense, with every sentence carrying distinct value and the most operationally urgent fact about API-key access front-loaded. It could be broken into clearer sections for scannability, but there is no filler or repetition.

Shorter descriptions cost fewer tokens and are easier for agents to parse. Every sentence should earn its place.

Completeness4/5

Given the tool's complexity, does the description cover enough for an agent to succeed on first attempt?

For a tool with no output schema and no annotations, the description covers the main returned elements (resolution, product codes, risk table, sample sizes), the key caveats, and the accepted input forms. The notable gap is that all parameters are optional in the schema while the description never explicitly states that exactly one of the three inputs should be supplied.

Complex tools with many parameters or behaviors need more documentation. Simple tools need less. This dimension scales expectations accordingly.

Parameters5/5

Does the description clarify parameter syntax, constraints, interactions, or defaults beyond what the schema provides?

The input schema already documents all three parameters, but the description adds substantial meaning: naming conventions, US/UK spelling resolution, no-brand/no-use guidance, how ambiguous names are resolved and reported, and the suggested follow-up call with gmdn_code. This goes well beyond the schema's example values.

Input schemas describe structure but not intent. Descriptions should explain non-obvious parameter relationships and valid value ranges.

Purpose5/5

Does the description clearly state what the tool does and how it differs from similar tools?

The description names a concrete verb and resource: it gives a classification view of a device type, enumerating the GMDN hierarchy, FDA product-code mappings with counts, and per-market risk classes with sample sizes. This is specific enough to distinguish the tool from all sibling tools without requiring additional schema inspection.

Agents choose between tools based on descriptions. A clear purpose with a specific verb and resource helps agents select the right tool.

Usage Guidelines4/5

Does the description explain when to use this tool, when not to, or what alternatives exist?

It tells the caller exactly what inputs are acceptable (a plain device name, GMDN code, or FDA product code) and how to phrase device_type, including avoiding brand names or use descriptions. It also explains how to follow up on ambiguous resolution via gmdn_code, but it does not explicitly name sibling tools or state when not to use this tool.

Agents often have multiple tools that could apply. Explicit usage guidance like "use X instead of Y when Z" prevents misuse.

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TDQS

A4.2/5.0
Disambiguation4/5

The tools cover clearly different queries—classification, predicate lineage, similar devices, market presence, registration details, timelines, recent entries, license holders, and coverage—so most are easy to distinguish. However, the get_registration family and get_coverage/get_market_coverage share naming patterns that could cause initial misselection despite thorough descriptions.

Naming Consistency4/5

All tool names follow a snake_case verb-first pattern, which is consistent and readable. The main weakness is that get_coverage and get_market_coverage are name-level near-duplicates, and the registration variants require careful reading to tell apart.

Tool Count5/5

Eleven tools is well within the ideal range for a specialized regulatory data domain, and each tool addresses a distinct part of the workflow. None feel redundant or superfluous, and the set is small enough for reliable agent routing.

Completeness4/5

The domain is covered broadly: manufacturer resolution, registration list/detail, market presence, timelines, recent activity, license holders, classification, US predicate history, and competitive devices are all present. Minor gaps such as a direct global device-type search across all manufacturers or bulk export can be worked around with existing tools.

Resources