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"Clear stream" Bante Alfa percutaneous puncture angioplasty catheter - Taiwan Registration 0fcba6f1af7dce7f2c7631c93bfdad26

Access comprehensive regulatory information for "Clear stream" Bante Alfa 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 0fcba6f1af7dce7f2c7631c93bfdad26 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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0fcba6f1af7dce7f2c7631c93bfdad26
Registration Details
Taiwan FDA Registration: 0fcba6f1af7dce7f2c7631c93bfdad26
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Device Details

"Clear stream" Bante Alfa percutaneous puncture angioplasty catheter
TW: โ€œๆธ…ๆตโ€็ญ็‰น้˜ฟ็ˆพ็™ผ็ถ“็šฎ็ฉฟๅˆบ่ก€็ฎกๆˆๅฝข่ก“ๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

0fcba6f1af7dce7f2c7631c93bfdad26

DHA00602415508

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, 2022

Apr 12, 2024

Cancellation Information

Logged out

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