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"Person" ASICS drug-releasing coronary bifurcation stent system - Taiwan Registration 45a274e2fd50f3d133145c71c9f68d54

Access comprehensive regulatory information for "Person" ASICS drug-releasing coronary bifurcation stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 45a274e2fd50f3d133145c71c9f68d54 and manufactured by BIOSENSORS EUROPE SA;; BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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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45a274e2fd50f3d133145c71c9f68d54
Registration Details
Taiwan FDA Registration: 45a274e2fd50f3d133145c71c9f68d54
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Device Details

"Person" ASICS drug-releasing coronary bifurcation stent system
TW: โ€œๆŸ็››โ€ไบž็‘Ÿๅฃซ่—ฅ็‰ฉ้‡‹ๆ”พๅž‹ๅ† ็‹€ๅ‹•่„ˆๅˆ†ๅ‰ๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

45a274e2fd50f3d133145c71c9f68d54

DHA05602594601

Product Details

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

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

import

Dates and Status

May 22, 2014

May 22, 2019

Jun 07, 2022

Cancellation Information

Logged out

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