Vi ống thông can thiệp mạch máu - Vietnam Registration 2401075ĐKLH/BYT-HTTB
Access comprehensive regulatory information for Vi ống thông can thiệp mạch máu 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 2401075ĐKLH/BYT-HTTB and manufactured by KANEKA Medix Corporation Kanagawa Plant. The authorized representative in Vietnam is CÔNG TY TNHH IMPORT MEDI VIỆT NAM.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including MicroVention Costa Rica, S.R.L.; MicroVention, Inc., MicroVention, Inc., and 5 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
2401075ĐKLH/BYT-HTTB
000.00.04.G18-231113-0022
Mizuki
MZ14-135BM; MZ14-150BM; MZ14-135TM; MZ14-150TM
Technical Details
To diagnose or treat vascular disorders by injecting contrast media or drugs into a target lesion in the blood vessel. Additionally, the product is used to ensure the passage of the guidewire in patients with fatty blood vessels (arteries, veins, or shunts) where the passage of the guidewire is difficult.
Dates and Status
Jul 21, 2024
Vi ống thông can thiệp mạch máu
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