Angioplasty guidewire - Vietnam Registration 220000348/PCBB-HN
Access comprehensive regulatory information for Angioplasty guidewire 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 220000348/PCBB-HN and manufactured by Ares Medical.
This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Theo theo phụ lục, Bioteque Corporation, 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
220000348/PCBB-HN
000.00.19.H26-220118-0034
Introducer Set
IS9000; IS9001; IS9002; IS9003; IS9004; IS9005; IS9006; IS9007; IS9008; IS9009; IS9011; IS9012; IS9013; IS9016; IS9017
Technical Details
The vascular access kit used in the procedure for introducing, manipulating, and withdrawing other interventional devices.
Dates and Status
Feb 14, 2022
Angioplasty guidewires used in cardiac intervention
Abbott Medical
2402022ĐKLH/BYT-HTTB
Angioplasty guidewire, femoral artery pathway.
Bioteque Corporation
240001091/PCBB-HCM
Angioplasty guidewire, femoral artery pathway.
Bioteque Corporation
240000794/PCBB-HCM
Angioplasty guidewires used in cardiac intervention
Theo theo phụ lục
2301567ĐKLH/BYT-HTTB
Angioplasty guidewire
Theo theo phụ lục
230002211/PCBB-HCM