--- name: "mdr-745-specialist" description: EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, and EUDAMED integration. triggers: - MDR compliance - EU MDR - medical device classification - Annex VIII - technical documentation - clinical evaluation - PMCF - EUDAMED - UDI - notified body ---

MDR 2017/745 Specialist

EU MDR compliance patterns for medical device classification, technical documentation, and clinical evidence.

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Table of Contents

• Device Classification Workflow
• Technical Documentation
• Clinical Evidence
• Post-Market Surveillance
• EUDAMED and UDI
• Reference Documentation
• Tools

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Device Classification Workflow

Classify device under MDR Annex VIII:

1. Identify device duration (transient, short-term, long-term)
2. Determine invasiveness level (non-invasive, body orifice, surgical)
3. Assess body system contact (CNS, cardiac, other)
4. Check if active device (energy dependent)
5. Apply classification rules 1-22
6. For software, apply MDCG 2019-11 algorithm
7. Document classification rationale
8. Validation: Classification confirmed with Notified Body

Classification Matrix

| Factor | Class I | Class IIa | Class IIb | Class III | |--------|---------|-----------|-----------|-----------| | Duration | Any | Short-term | Long-term | Long-term | | Invasiveness | Non-invasive | Body orifice | Surgical | Implantable | | System | Any | Non-critical | Critical organs | CNS/cardiac | | Risk | Lowest | Low-medium | Medium-high | Highest |

Software Classification (MDCG 2019-11)

| Information Use | Condition Severity | Class | |-----------------|-------------------|-------| | Informs decision | Non-serious | IIa | | Informs decision | Serious | IIb | | Drives/treats | Critical | III |

Classification Examples

Example 1: Absorbable Surgical Suture

• Rule 8 (implantable, long-term)
• Duration: > 30 days (absorbed)
• Contact: General tissue
• Classification: Class IIb

Example 2: AI Diagnostic Software

• Rule 11 + MDCG 2019-11
• Function: Diagnoses serious condition
• Classification: Class IIb

Example 3: Cardiac Pacemaker

• Rule 8 (implantable)
• Contact: Central circulatory system
• Classification: Class III

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Technical Documentation

Prepare technical file per Annex II and III:

1. Create device description (variants, accessories, intended purpose)
2. Develop labeling (Article 13 requirements, IFU)
3. Document design and manufacturing process
4. Complete GSPR compliance matrix
5. Prepare benefit-risk analysis
6. Compile verification and validation evidence
7. Integrate risk management file (ISO 14971)
8. Validation: Technical file reviewed for completeness

Technical File Structure

ANNEX II TECHNICAL DOCUMENTATION
├── Device description and UDI-DI
├── Label and instructions for use
├── Design and manufacturing info
├── GSPR compliance matrix
├── Benefit-risk analysis
├── Verification and validation
└── Clinical evaluation report

GSPR Compliance Checklist

| Requirement | Evidence | Status | |-------------|----------|--------| | Safe design (GSPR 1-3) | Risk management file | ☐ | | Chemical properties (GSPR 10.1) | Biocompatibility report | ☐ | | Infection risk (GSPR 10.2) | Sterilization validation | ☐ | | Software requirements (GSPR 17) | IEC 62304 documentation | ☐ | | Labeling (GSPR 23) | Label artwork, IFU | ☐ |

Conformity Assessment Routes

| Class | Route | NB Involvement | |-------|-------|----------------| | I | Annex II self-declaration | None | | Is/Im | Annex II + IX/XI | Sterile/measuring aspects | | IIa | Annex II + IX or XI | Product or QMS | | IIb | Annex IX + X or X + XI | Type exam + production | | III | Annex IX + X | Full QMS + type exam |

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Clinical Evidence

Develop clinical evidence strategy per Annex XIV:

1. Define clinical claims and endpoints
2. Conduct systematic literature search
3. Appraise clinical data quality
4. Assess equivalence (technical, biological, clinical)
5. Identify evidence gaps
6. Determine if clinical investigation required
7. Prepare Clinical Evaluation Report (CER)
8. Validation: CER reviewed by qualified evaluator

Evidence Requirements by Class

| Class | Minimum Evidence | Investigation | |-------|------------------|---------------| | I | Risk-benefit analysis | Not typically required | | IIa | Literature + post-market | May be required | | IIb | Systematic literature review | Often required | | III | Comprehensive clinical data | Required (Article 61) |

Clinical Evaluation Report Structure

CER CONTENTS
├── Executive summary
├── Device scope and intended purpose
├── Clinical background (state of the art)
├── Literature search methodology
├── Data appraisal and analysis
├── Safety and performance conclusions
├── Benefit-risk determination
└── PMCF plan summary

Qualified Evaluator Requirements

• Medical degree or equivalent healthcare qualification
• 4+ years clinical experience in relevant field
• Training in clinical evaluation methodology
• Understanding of MDR requirements

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Post-Market Surveillance

Establish PMS system per Chapter VII:

1. Develop PMS plan (Article 84)
2. Define data collection methods
3. Establish complaint handling procedures
4. Create vigilance reporting process
5. Plan Periodic Safety Update Reports (PSUR)
6. Integrate with PMCF activities
7. Define trend analysis and signal detection
8. Validation: PMS system audited annually

PMS System Components

| Component | Requirement | Frequency | |-----------|-------------|-----------| | PMS Plan | Article 84 | Maintain current | | PSUR | Class IIa and higher | Per class schedule | | PMCF Plan | Annex XIV Part B | Update with CER | | PMCF Report | Annex XIV Part B | Annual (Class III) | | Vigilance | Articles 87-92 | As events occur |

PSUR Schedule

| Class | Frequency | |-------|-----------| | Class III | Annual | | Class IIb implantable | Annual | | Class IIb | Every 2 years | | Class IIa | When necessary |

Serious Incident Reporting

| Timeline | Requirement | |----------|-------------| | 2 days | Serious public health threat | | 10 days | Death or serious deterioration | | 15 days | Other serious incidents |

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EUDAMED and UDI

Implement UDI system per Article 27:

1. Obtain issuing entity code (GS1, HIBCC, ICCBBA)
2. Assign UDI-DI to each device variant
3. Assign UDI-PI (production identifier)
4. Apply UDI carrier to labels (AIDC + HRI)
5. Register actor in EUDAMED
6. Register devices in EUDAMED
7. Upload certificates when available
8. Validation: UDI verified on sample labels

EUDAMED Modules

| Module | Content | Actor | |--------|---------|-------| | Actor | Company registration | Manufacturer, AR | | UDI/Device | Device and variant data | Manufacturer | | Certificates | NB certificates | Notified Body | | Clinical Investigation | Study registration | Sponsor | | Vigilance | Incident reports | Manufacturer | | Market Surveillance | Authority actions | Competent Authority |

UDI Label Requirements

Required elements per Article 13:

• [ ] UDI-DI (device identifier)
• [ ] UDI-PI (production identifier) for Class II+
• [ ] AIDC format (barcode/RFID)
• [ ] HRI format (human-readable)
• [ ] Manufacturer name and address
• [ ] Lot/serial number
• [ ] Expiration date (if applicable)

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Reference Documentation

MDR Classification Guide

references/mdr-classification-guide.md contains:

• Complete Annex VIII classification rules (Rules 1-22)
• Software classification per MDCG 2019-11
• Worked classification examples
• Conformity assessment route selection

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