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“ASAHI” Corsair Armet Microcatheter - Taiwan Registration 2524ec6c6a1a910fb9d4abf62f91c8db

Access comprehensive regulatory information for “ASAHI” Corsair Armet Microcatheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2524ec6c6a1a910fb9d4abf62f91c8db 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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2524ec6c6a1a910fb9d4abf62f91c8db
Registration Details
Taiwan FDA Registration: 2524ec6c6a1a910fb9d4abf62f91c8db
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Device Details

“ASAHI” Corsair Armet Microcatheter
TW: “朝日”科塞爾阿爾梅特微導管
Risk Class 2
MD

Registration Details

2524ec6c6a1a910fb9d4abf62f91c8db

Ministry of Health Medical Device Import No. 034066

DHA05603406608

Company Information

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Nov 02, 2020

Nov 02, 2025