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mdr-745-specialist

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.

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技能说明

MDR 2017/745 Specialist

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


Table of Contents


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 -...

来源信息

Source
github
Repository
openclaw/skills
Path
skills/alirezarezvani/mdr-745-specialist
Version
—
Commit
45be2b372e4f24e3c9796e200b1b9832c2141ed9
分类来源
rules
状态
active
可见性
public

这些信息来自收录时的来源分析,可能滞后;使用前请核对最新来源文件。

来源内容

SKILL.md
# MDR 2017/745 Specialist

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

---

## Table of Contents

- [Device Classification Workflow](#device-classification-workflow)
- [Technical Documentation](#technical-documentation)
- [Clinical Evidence](#clinical-evidence)
- [Post-Market Surveillance](#post-market-surveillance)
- [EUDAMED and UDI](#eudamed-and-udi)
- [Reference Documentation](#reference-documentation)
- [Tools](#tools)

---

## 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**
-...

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