Pulmonary Artery Dilatation Guiding Catheter
Vietnam·Risk Class TTBYT Loại D·NuCLEUS-X Catheter (NuCLEUS-X Percutaneous Transluminal Valvuloplasty Catheter)·Numed, Inc.·Registered Apr 10, 2024- Analysis ID
- 2400437ĐKLH/BYT-HTTB
- Submission ID
- 19011014/ĐKLH-BYT-TB-CT
- Product Type
- NuCLEUS-X Catheter (NuCLEUS-X Percutaneous Transluminal Valvuloplasty Catheter)
- Product Code
- PVN400, PVN401, PVN402, PVN403, PVN404, PVN405, PVN406, PVN407, PVN408, PVN409, PVN410, PVN411, PVN412, PVN413, PVN414, PVN415, PVN416, PVN417.
- Manufacturer
- Numed, Inc.
- Manufacturer Country
- Theo theo phụ lục
- Product Owner
- Numed, Inc.
- Authorized Representative
- CÔNG TY TNHH DƯỢC PHẨM VÀ TRANG THIẾT BỊ Y TẾ HOÀNG ĐỨC
- Intended Use
- 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.
- Registration Date
- Apr 10, 2024
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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.