Taiwan FDA registration 5c529a537df77afa135a0472dadac3ef
“Hexacath” Merak LD PTA Dilatation Catheter
TW: “海斯凱” 翼星周邊血管球囊擴張導管
Taiwan·Risk Class 2·MD·Hexacath·Registered Sep 07, 2021 – Sep 07, 2026ActiveRegistration details
- Analysis ID
- 5c529a537df77afa135a0472dadac3ef
- License Form
- Ministry of Health Medical Device Import No. 034852
- Customs Code
- DHA05603485203
Company information
- Manufacturer
- Hexacath
- Manufacturer Country
- France
- Authorized Representative
- CATHERINE CONSULTANTS CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 07, 2021
- Expiry Date
- Sep 07, 2026
About this record
Access comprehensive regulatory information for “Hexacath” Merak LD PTA Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5c529a537df77afa135a0472dadac3ef and manufactured by Hexacath. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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