Vietnam MOH registration 2403521ĐKLH/BYT-HTTB
Vi ống thông dùng trong can thiệp tim mạch
Registration details
- Analysis ID
- 2403521ĐKLH/BYT-HTTB
- Submission ID
- 18007633/ĐKLH-BYT-TB-CT
- Product Type
- ReCross
- Product Code
- RC1414025 (mã đặt hàng 451671)
Company information
- Manufacturer
- IMDS Operations B.V.
- Manufacturer Country
- NETHERLANDS
- Product Owner
- IMDS Operations B.V.
- Authorized Representative
- VĂN PHÒNG ĐẠI DIỆN BIOTRONIK ASIA PACIFIC PTE. LTD. TẠI THÀNH PHỐ HỒ CHÍ MINH
Technical details
- Intended Use
- ReCross, which is coated with hydrophilic material, is designed to facilitate the delivery of the guidewire during the coronary and/or peripheral vascular access procedure, while simultaneously enabling the transfer of the interventional guidewire and providing an additional lumen for the injection of the diagnostic contrast media.
Dates and status
- Registration Date
- Nov 14, 2024
About this record
Access comprehensive regulatory information for Vi ống thông dùng trong can thiệp tim mạch in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TBYT Loại D medical device is registered under number 2403521ĐKLH/BYT-HTTB and manufactured by IMDS Operations B.V.. The authorized representative in Vietnam is VĂN PHÒNG ĐẠI DIỆN BIOTRONIK ASIA PACIFIC PTE. LTD. TẠI THÀNH PHỐ HỒ CHÍ MINH.
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.
Free DatabasePowered by Pure Global AI300,000+ Devices