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Guiding Wire - Vietnam Registration 220003571/PCBB-HCM

Access comprehensive regulatory information for Guiding Wire 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 220003571/PCBB-HCM and manufactured by ENDO-FLEX GmbH.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Theo theo phụ lục, DLR Medikal San. ve Dıs Tic. Ltd. Sti., 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.

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220003571/PCBB-HCM
Registration Details
Vietnam MOH Registration: 220003571/PCBB-HCM
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Device Details

Guiding Wire
VN: Dây dẫn hướng
Risk Class TTBYT Loại B

Registration Details

220003571/PCBB-HCM

000.00.19.H29-221108-0024

21525400; 21535400; 21535500; 21538260;

21525400; 21535400; 21535500; 21538260;

Company Information

Technical Details

The guidewire, which is capable of resisting kinking, is used to guide the soft endoscopic instruments, which are used to guide the instruments to the area to be treated in the human body.

Dates and Status

Nov 09, 2022