ios-qa
ios-qa
【效率与协作】Live-device iOS QA for SwiftUI apps. (gstack)
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ruview-hardware-setup
ruview-hardware-setup
【开发与工程】ESP32-S3 / ESP32-C6 firmware build, flash, WiFi provisioning, and serial monitoring for RuView CSI sensing nodes. Use when setting up physical hardware, reflashing a node, or debugging a device that isn't streaming CSI.
favicons
favicons
【开发与工程】Use when reviewing templates, rendered HTML, or shared components related to Implement favicons for all devices. Validate the final browser-facing markup, not just the source framework abstraction.
mobile-testing
mobile-testing
【文档与办公】Use when reviewing CI coverage, automated checks, or test strategy related to Test on real mobile devices and viewports. Focus on whether the rule is continuously verified, not just documented.
scheduler-yield
scheduler-yield
【数据与研究】Use when reviewing JavaScript that performs synchronous loops over large datasets, recursive tree traversals, or bulk DOM updates that may exceed 50 ms on mid-range devices.
iso-standards-readiness
iso-standards-readiness
【文档与办公】Prepares and structurally reviews readiness evidence for ISO management-system and laboratory-competence standards - ISO 13485 medical device QMS, ISO 14971 device risk management, ISO/IEC 17025 testing and calibration laboratories, and ISO 15189 medical laboratories. Use when organizing declared scope, controlled documents, risk-management files, sc…
neurokit2
neurokit2
【数据与研究】Builds and audits reproducible NeuroKit2 research workflows for physiological time-series preprocessing, event/interval analysis, multimodal alignment, variability, and complexity. Use when code imports neurokit2 or needs its current APIs, schemas, and method-aware validation—not for diagnosis or device validation.
pylabrobot
pylabrobot
【开发与工程】Develops and reviews PyLabRobot lab-automation resources, liquid-handling plans, offline simulations, and supported-device integrations. Supports PyLabRobot protocols and API questions; keep physical execution behind an explicit operator safety gate.
appium-skill
appium-skill
【开发与工程】Generates production-grade Appium mobile automation scripts for Android and iOS in Java, Python, or JavaScript. Supports real device and emulator testing locally and on TestMu AI cloud with 100+ real devices.
apple-notes-search
apple-notes-search
【开发与工程】Semantic + keyword search and connection-discovery across the user's own Apple Notes via the apple-notes MCP server. Use when the user wants to find, recall, or synthesize something from their notes, or surface non-obvious bridges/related notes. macOS, on-device.
cloudflare-zero-trust
cloudflare-zero-trust
【部署与运维】Protect internal apps with Cloudflare Access, device posture, and Zero Trust policies.
fda-medtech-compliance-auditor
fda-medtech-compliance-auditor
【开发与工程】Expert AI auditor for Medical Device (SaMD) compliance, IEC 62304, and 21 CFR Part 820. Reviews DHFs, technical files, and software validation.
mdm-device-management
mdm-device-management
【效率与协作】Manage and secure company devices with MDM solutions
premium-3d-website
premium-3d-website
【开发与工程】Guidelines for building premium 3D websites, focusing on custom WebGL shaders, post-processing, physics-based interactions, smooth animations, preloaders, and device optimization.
exploring-live-traffic
exploring-live-traffic
【数据与研究】Inspects PostHog Web analytics Live tab data — current users online, last-30-minutes pageviews, top pages, referrers, devices, browsers, countries, bot traffic, and the per-minute bot/users charts. Use when the user asks "who is on my site right now?", "what is happening live?", "what bots are crawling me?", asks about the "live tab" / "live dashboar…
capa-officer
capa-officer
【数据与研究】CAPA system management for medical device QMS. Covers root cause analysis, corrective action planning, effectiveness verification, and CAPA metrics. Use when running CAPA investigations, 5-Why analysis, fishbone diagrams, root cause determination, corrective action tracking, effectiveness verification, or CAPA program optimization.
fda-consultant-specialist
fda-consultant-specialist
【效率与协作】FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QMSR (21 CFR 820, which incorporates ISO 13485:2016 by reference since 2026-02-02; formerly QSR) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QMSR, QSR, ISO 13485 for FDA, prema…
mdr-745-specialist
mdr-745-specialist
【文档与办公】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, Art. 86 PSUR schedules, and EUDAMED integration. Use when classifying a medical device under MDR, buildi…
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