Results for “medical-device”
11 skillsMdr 745 Specialist
Classify medical devices under EU MDR 2017/745, build technical documentation, plan clinical evaluations, and manage post-market surveillance and EUDAMED integration.
20.4k · bundle
Qms Audit Expert
Provides ISO 13485 internal audit methodology for medical device quality management systems, covering audit planning, execution, nonconformity classification, and external audit preparation.
20.4k · bundle
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Iso 13485 Certification
Prepare ISO 13485:2016 certification documentation for medical device Quality Management Systems, including gap analysis, template-based document creation, and compliance checklists.
30.2k · bundle
116 Mdr 27c00614
Classifies medical devices under EU MDR 2017/745 Annex VIII rules, including software per MDCG 2019-11, with examples and conformity assessment routes.
7 · bundle
Doubao Medical Report
必须在用户需要医学报告解读时使用。包括:用户上传体检报告、检验报告、检查单、化验单、血常规/尿常规/生化/肝肾功能/血脂血糖等检验检查图片、照片、截图、PDF、文档、表格或文件;用户只发报告图片/附件且没有文字说明;用户说“帮我看看”“看下这个报告”“这个结果正常吗”“有什么问题”“报告怎么解读”;用户表达体检报告解读、医院报告解读、影像/超声/CT/MRI/内镜/病理报告解读等需求。用于梳理报告内容,解释异常指标和检查发现,识别需要关注的风险信号,并给出就医沟通、复查随访、观察监测和生活方式管理建议。
9 · bundle
Doctor
System diagnostics and health checks for Diverga plugin. OpenClaw-style Check-Report-Fix pattern with 5-layer diagnostics. Triggers: /diverga:doctor, diverga doctor, system check, diagnose, 진단
1k
Songsee
Generate spectrograms and audio feature visualizations (mel, chroma, MFCC, tempogram, etc.) from audio files via CLI. Useful for audio analysis, music production debugging, and visual documentation.
0 · bundle
Ehr Template
Design EHR templates for clinical documentation. TRIGGERS - Use when user needs help with ehr-template related tasks.
3
Scientific Slides
Build visually engaging scientific slide decks for conferences, seminars, defenses, and research talks with structured planning, design templates, and automated image generation.
30.2k · bundle
Dbs Report
Merges multiple diagnosis snapshots from dbs-save into a single, timestamped Markdown report organized by topic.
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.
0 · bundle