High-pressure percutaneous vascular intervention - Vietnam Registration 2400479ĐKLH/BYT-HTTB
Access comprehensive regulatory information for High-pressure percutaneous vascular intervention in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại D medical device is registered under number 2400479ĐKLH/BYT-HTTB and manufactured by Goodman Co.,Ltd. The authorized representative in Vietnam is CÔNG TY TNHH NIPRO SALES VIỆT NAM.
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.
Device Details
Registration Details
2400479ĐKLH/BYT-HTTB
000.00.04.G18-221226-0047
Theo theo phụ lục
Theo phụ lục
Technical Details
The device is designed to dilate narrow vessels (arteries, veins, or conduits) during the process of percutaneous transluminal angioplasty (PTA) or post-stent dilation. However, it does not include the coronary arteries and the brain vessels.
Dates and Status
Apr 10, 2024

