“ASAHI” Peripheral Guide Wire - Taiwan Registration 2ef7d37efda4a9ef22d9a91591624b8a
Access comprehensive regulatory information for “ASAHI” Peripheral Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2ef7d37efda4a9ef22d9a91591624b8a 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.
Device Details
Registration Details
2ef7d37efda4a9ef22d9a91591624b8a
Ministry of Health Medical Device Import No. 030634
DHA05603063402
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
Dec 28, 2017
Dec 28, 2027

