TheBotique

MedXpert 全球法规连接器

An MCP connector for medical device regulatory retrieval, covering MDR/CE, FDA 510(k), UDI, STED, classification, and global registration pathways. Agents query the local read-only NMPA/FDA/MDR/PMDA 27-hub regulation knowledge base via MCP—no network egress, no credentials. 医疗器械注册法规检索 MCP 连接器,覆盖 MDR

as observed 2026-11-06T15:44:01.797Z
Identifier
medxpert-reg-connector
Source
ClawHub
Version observed
1.0.3
Source repository
not published
Repository observation
No source repository listed
First observed here
2026-08-29T23:02:09.653Z
Observations recorded
2
Installs (reported upstream)
1
Weekly downloads (upstream)
434
Declared license
MIT-0

Observation history

2026-11-06T15:44:01.797Z

Fields that differed: license changelog description latestVersion summary

FieldBeforeAfter
license null "MIT-0"
changelog "MedXpert 全球法规连接器 MCP 运行时:本地只读检索 27 枢纽法规知识库,4 工具,零凭据零外发,与 medxpert-reg-hub 互补。" "上架标准 v1.0 收尾:简介双语英文在前、补 tags、包内附 llms.txt 并给出直达链接。技能逻辑未改动。"
description "医疗器械注册法规检索 MCP 连接器,覆盖 MDR/CE、FDA 510(k)、UDI、STED、分类界定、全球注册路径等场景;agent 通过 MCP 本地只读检索 NMPA/FDA/MDR/PMDA 等 27 枢纽法规知识库,无需联网外发、无需凭据。" null
latestVersion "1.0.0" "1.0.3"
summary "医疗器械注册法规检索 MCP 连接器,覆盖 MDR/CE、FDA 510(k)、UDI、STED、分类界定、全球注册路径等场景;agent 通过 MCP 本地只读检索 NMPA/FDA/MDR/PMDA 等 27 枢纽法规知识库,无需联网外发、无需凭据。" "An MCP connector for medical device regulatory retrieval, covering MDR/CE, FDA 510(k), UDI, STED, classification, and global registration pathways. Agents query the local read-onl

Correction

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