Pulmonary Artery Dilatation Guiding Catheter - Vietnam Registration 2400437ĐKLH/BYT-HTTB
Access comprehensive regulatory information for Pulmonary Artery Dilatation Guiding Catheter 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 2400437ĐKLH/BYT-HTTB and manufactured by Numed, Inc.. The authorized representative in Vietnam is CÔNG TY TNHH DƯỢC PHẨM VÀ TRANG THIẾT BỊ Y TẾ HOÀNG ĐỨC.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Numed, Inc., and 1 recent registrations in the same category. 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
2400437ĐKLH/BYT-HTTB
19011014/ĐKLH-BYT-TB-CT
NuCLEUS-X Catheter (NuCLEUS-X Percutaneous Transluminal Valvuloplasty Catheter)
PVN400, PVN401, PVN402, PVN403, PVN404, PVN405, PVN406, PVN407, PVN408, PVN409, PVN410, PVN411, PVN412, PVN413, PVN414, PVN415, PVN416, PVN417.
Technical Details
It is designated for the treatment of double-lumen stenosis and the cutaneous aorta. This product is particularly designated for locations where the balloon positioning process during the injection phase is difficult.
Dates and Status
Apr 10, 2024