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"Clear flow" Bantflorian percutaneous puncture angioplasty catheter - Taiwan Registration 6b25e4ba72e1ba93f57885dd159b4d63

Access comprehensive regulatory information for "Clear flow" Bantflorian percutaneous puncture angioplasty catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b25e4ba72e1ba93f57885dd159b4d63 and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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6b25e4ba72e1ba93f57885dd159b4d63
Registration Details
Taiwan FDA Registration: 6b25e4ba72e1ba93f57885dd159b4d63
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Device Details

"Clear flow" Bantflorian percutaneous puncture angioplasty catheter
TW: โ€œๆธ…ๆตโ€็ญ็‰นๅผ—ๆด›้‡Œๅฎ‰็ถ“็šฎ็ฉฟๅˆบ่ก€็ฎกๆˆๅฝข่ก“ๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

6b25e4ba72e1ba93f57885dd159b4d63

DHA00602415702

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Nov 05, 2012

Nov 05, 2017

Dec 20, 2019

Cancellation Information

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