Taiwan FDA registration 2524ec6c6a1a910fb9d4abf62f91c8db
“ASAHI” Corsair Armet Microcatheter
TW: “朝日”科塞爾阿爾梅特微導管
Taiwan·Risk Class 2·MD·ASAHI INTECC(THAILAND) CO., LTD·Registered Nov 02, 2020 – Nov 02, 2025ExpiredRegistration details
- Analysis ID
- 2524ec6c6a1a910fb9d4abf62f91c8db
- License Form
- Ministry of Health Medical Device Import No. 034066
- Customs Code
- DHA05603406608
Company information
- Manufacturer
- ASAHI INTECC(THAILAND) CO., LTD
- Manufacturer Country
- Thailand
- Authorized Representative
- ASAHI INTECC CO.,LTD. TAIWAN BRANCH (JAPAN)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 02, 2020
- Expiry Date
- Nov 02, 2025
About this record
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.
Free DatabasePowered by Pure Global AI89,000+ Devices