# Model card (draft)

**Product / version:**  
**Model / artifact ID:**  
**Date:**  
**Owner (name, role):**

## Intended use

- Medical purpose (one sentence):
- Population / setting:
- Non-goals (what the model must not be used for):

## Model type and role

- Architecture family (e.g. classifier, regressor, LLM-assisted documentation):
- Human oversight (e.g. mandatory review threshold):

## Training and tuning data (summary)

- Data sources (high level; link to data card):
- Labeling approach:
- Time window and geography:
- Known gaps or biases:

## Performance

- Primary metrics and thresholds:
- Subgroup / SGBA Plus considerations:
- Failure modes and unresolvable errors (if any):

## Monitoring and update policy

- Drift metrics:
- PCCP bounds (if applicable):
- Rollback triggers:

## Regulatory and risk links

- Related hazards / ISO 14971 IDs:
- Cyber / logging considerations:

## Transparency

- User-facing explanations or confidence policy:
