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“ASAHI” EXTENSION WIRE - Taiwan Registration df5640aca3b61e36226a71ac7a381e69

Access comprehensive regulatory information for “ASAHI” EXTENSION WIRE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df5640aca3b61e36226a71ac7a381e69 and manufactured by ASAHI INTECC(THAILAND) CO., LTD. The authorized representative in Taiwan is ASAHI INTECC CO.,LTD. TAIWAN BRANCH (JAPAN).

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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df5640aca3b61e36226a71ac7a381e69
Registration Details
Taiwan FDA Registration: df5640aca3b61e36226a71ac7a381e69
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Device Details

“ASAHI” EXTENSION WIRE
TW: “朝日”冠狀動脈延長導引線
Risk Class 2
MD

Registration Details

df5640aca3b61e36226a71ac7a381e69

Ministry of Health Medical Device Import No. 025470

DHA05602547001

Company Information

Product Details

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

E Cardiovascular devices

E1330 Catheter Lead

Imported from abroad

Dates and Status

Nov 25, 2013

Nov 25, 2028