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"Asahi" quick-swap percutaneous coronary angioplasty catheter - Taiwan Registration f943b1c51bfc349b3a4d2a769cd0bb2c

Access comprehensive regulatory information for "Asahi" quick-swap percutaneous coronary angioplasty catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number f943b1c51bfc349b3a4d2a769cd0bb2c and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. The authorized representative in Taiwan is HSIN TUNG MEDICAL 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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f943b1c51bfc349b3a4d2a769cd0bb2c
Registration Details
Taiwan FDA Registration: f943b1c51bfc349b3a4d2a769cd0bb2c
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Device Details

"Asahi" quick-swap percutaneous coronary angioplasty catheter
TW: "ๆœๆ—ฅ" ๅฟซ้€ŸๆŠฝๆ›ๅผ็ถ“็šฎๅ† ็‹€ๅ‹•่„ˆ่ก€็ฎกๆˆๅž‹่ก“ๅฐŽ็ฎก
Cancelled

Registration Details

f943b1c51bfc349b3a4d2a769cd0bb2c

DHA00601155302

Company Information

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Jun 22, 2005

Jun 22, 2010

Nov 09, 2012

Cancellation Information

Logged out

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