§ COMPARE REGULATORS
TGA vs Medsafe：医疗器械监管对比
对比 TGA (Australia) 与 Medsafe (New Zealand) 的医疗器械注册路径、分类和监管要求。
TGA
澳大利亚治疗产品管理局
Australia
TGA根据1989年《治疗产品法》监管澳大利亚医疗器械。澳大利亚使用与GHTF/IMDRF一致的风险分类体系。TGA是MDSAP参与机构。…
CLASSES
Class I, IIa, IIb, III, AIMD
PATHWAY
ARTG inclusion via conformity assessment
KEY FUNCTIONS
- ▸ARTG注册
- ▸合格性评估
- ▸MDSAP参与
- ▸不良事件报告
- ▸上市后监管
Medsafe
Medsafe — New Zealand医疗器械监管机构
New Zealand
Medsafe是New Zealand负责医疗器械监管的国家监管机构，负责器械注册、市场监督和不良事件报告。…
CLASSES
Class I, IIa, IIb, III
PATHWAY
Medsafe registration
KEY FUNCTIONS
- ▸器械注册
- ▸市场监督
- ▸不良事件报告
- ▸进出口管控
MedFlux monitors both TGA and Medsafe in real time — every regulatory change, safety alert, and market signal delivered in under 90 seconds.
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