Vietnam MOH registration 240000011/PCBB-HN
Kim luồn an toàn dùng trong chạy thận nhân tạo
Registration details
- Analysis ID
- 240000011/PCBB-HN
- Submission ID
- 000.00.19.H26-231215-0016
- Product Type
- Theo theo phụ lục
- Product Code
- Theo phụ lục
Company information
- Manufacturer
- B. Braun Melsungen
- Manufacturer Country
- Theo theo phụ lục
- Product Owner
- B. Braun Melsungen
- Authorized Representative
- CÔNG TY TNHH B. BRAUN VIỆT NAM
Technical details
- Intended Use
- Diacan® Flex is used to create an access route into the peripheral blood vessel system (the arteriovenous fistula, the arteriovenous graft) by the fistulization procedure for extracorporeal blood purification therapies.
Dates and status
- Registration Date
- Jan 05, 2024
About this record
Access comprehensive regulatory information for Kim luồn an toàn dùng trong chạy thận nhân tạo in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 240000011/PCBB-HN and manufactured by B. Braun Melsungen. 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.
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