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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.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.

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240001359/PCBB-HN
Registration Details
Vietnam MOH Registration: 240001359/PCBB-HN
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Device Details

Single-use directional guide wire
VN: Dây dẫn hướng dùng một lần
Risk Class TTBYT Loại B

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

Company Information

Zhejiang Soudon Medical Technology Co., Ltd

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