Taiwan FDA registration fdd565f77b7817474624eab579469104
“ASAHI” Hyperion Coronary Guide Catheter
TW: “朝日”海伯利安冠狀血管導引導管
Taiwan·Risk Class 2·MD·ASAHI INTECC(THAILAND) CO., LTD·Registered Oct 12, 2017 – Oct 12, 2027ActiveRegistration details
- Analysis ID
- fdd565f77b7817474624eab579469104
- License Form
- Ministry of Health Medical Device Import No. 030277
- Customs Code
- DHA05603027701
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
- Oct 12, 2017
- Expiry Date
- Oct 12, 2027
About this record
Access comprehensive regulatory information for “ASAHI” Hyperion Coronary Guide Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdd565f77b7817474624eab579469104 and manufactured by ASAHI INTECC(THAILAND) CO., LTD. The authorized representative in Taiwan is ASAHI INTECC CO.,LTD. TAIWAN BRANCH (JAPAN).
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