Single-use directional guide wire - Vietnam Registration 240001359/PCBB-HN
Access comprehensive regulatory information for Single-use directional guide wire in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 240001359/PCBB-HN and manufactured by Zhejiang Soudon Medical Technology Co., Ltd. The authorized representative in Vietnam is CÔNG TY TNHH THIẾT BỊ Y TẾ MINH THIÊN.
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Device Details
Registration Details
240001359/PCBB-HN
000.00.19.H26-240605-0010
SD-06-89-A450S, SD-06-89-A450J, SD-06-89-A260S, SD-06-89-A260J
Technical Details
The single-use guidewire is intended for use in selective bile duct stenting, including common bile ducts, cystic ducts, right and left hepatic ducts. The single-use guidewire is designed for use in endoscopic biliary procedures to deliver and exchange the stents.
Dates and Status
Jun 07, 2024

