Zhejiang CuraWay Medical Technology Co, Ltd

Room 106, Building 1, No. 600, 21st Avenue, Baiyang Sub-district, Qiantang New District, Hangzhou, China, 310018

17 devices* 33 registrations
✕ Canada (Health Canada)
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Devices

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Device Name US UK CA AU EU
Automamatic Core Biopsy Instrument Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Automatic Core Biopsy Instrument Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Registered with AU (TGA) Registered with EU (EUDAMED)
Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy Needle Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Bone Marrow Biopsy Needle Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Breast Lesion Localization Wire Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Cura RF Electrode Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Disposable Biopsy Needle Registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Disposable Coaxial Biopsy Needle Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Endovenous Radiofrequency Catheter Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Endovenous Radiofrequency Generator Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Irreversible Electroporation Ablation Generator Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Irreversible Electroporation Probe Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Radiofrequency Generator Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Radiofrequency Generator System, Cura RF Electrode Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Semi-Automatic Core Biopsy Instrument Not registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)

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