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“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.

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2ef7d37efda4a9ef22d9a91591624b8a
Registration Details
Taiwan FDA Registration: 2ef7d37efda4a9ef22d9a91591624b8a
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Device Details

“ASAHI” Peripheral Guide Wire
TW: “朝日”周邊血管導引線
Risk Class 2
MD

Registration Details

2ef7d37efda4a9ef22d9a91591624b8a

Ministry of Health Medical Device Import No. 030634

DHA05603063402

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

Dec 28, 2017

Dec 28, 2027