io.tooloracle/healthguard

up checked 2026-11-11T00:37:42.329Z

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Publisher-provided description

HealthGuard - 12-tool health/medical AI safety MCP: PII redaction, HIPAA, GDPR Art.9.

Summary by lookupd

Offers EU and US healthcare regulatory checks: medical device classification, drug interaction screening, GDPR and HIPAA compliance…

Install

Claude Code, remote (streamable-http)

claude mcp add --transport http healthguard https://tooloracle.io/health/mcp/

Codex, remote (streamable-http)

codex mcp add healthguard --url https://tooloracle.io/health/mcp/

Cursor, remote (streamable-http) → .cursor/mcp.json

{
  "mcpServers": {
    "healthguard": {
      "url": "https://tooloracle.io/health/mcp/"
    }
  }
}

Other clients: docs. Or tell your agent: Set up lookupd for me: read https://lookupd.com/agent.md and follow it.

Tools (12 tools)

Publisher-provided text

• mdr_compliance_check EU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance sco
• ivdr_check EU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.
• device_classification MDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.
• udi_validate Validate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).
• drug_interaction Basic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.
• icd10_lookup ICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).
• adverse_event_report Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.
• gdpr_health_check GDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.
• hipaa_vs_gdpr HIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.
• clinical_trial_phases Clinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.
• gmp_checklist Good Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.
• medical_calendar_eu EU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.

Details

• Version: 1.0.0
• Transports: streamable-http
• Uptime (7 days): 100%
• Median latency: 557 ms
• First indexed: 2026-11-01T10:03:31.235Z
• Last seen in registry: 2026-11-01T10:03:31.235Z
• Repository: https://github.com/ToolOracle/healthguard

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