Venous Thromboembolic Filtration Mesh - Vietnam Registration 2400987ĐKLH/BYT-HTTB
Access comprehensive regulatory information for Venous Thromboembolic Filtration Mesh 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 2400987ĐKLH/BYT-HTTB and manufactured by B. BRAUN MEDICAL. The authorized representative in Vietnam is CÔNG TY TNHH B. BRAUN 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
2400987ĐKLH/BYT-HTTB
17000664/ĐKLH-BYT-TB-CT
VenaTech® LP
04435125
Technical Details
The VenaTech® LP venous thromboembolic filtration mesh is indicated for patients at risk of long-term or permanent thromboembolism. Indications for placement of the filtration mesh include: - Patients contraindicated for anticoagulant therapy - Patients with complications from anticoagulant therapy - Patients who have failed or are not adequately responding to anticoagulation - Emergency treatment after severe pulmonary embolism when the expected benefit of conventional therapy is reduced despite effective filtration
Dates and Status
Jul 21, 2024