Taiwan FDA registration 8c6175146fe331de6bab2af1b55c494c
Honeytec balloon dilation catheter
TW: 悍耐得球囊擴張導管
Taiwan·Risk Class 2·BARD PERIPHERAL VASCULAR, INC.;; CLEARSTREAM TECHNOLOGIES LTD.·Registered Jun 25, 2024 – Jun 25, 2029ActiveRegistration details
- Analysis ID
- 8c6175146fe331de6bab2af1b55c494c
- Customs Code
- DHA05603723000
Company information
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Jun 25, 2024
- Expiry Date
- Jun 25, 2029
About this record
Access comprehensive regulatory information for Honeytec balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8c6175146fe331de6bab2af1b55c494c and manufactured by BARD PERIPHERAL VASCULAR, INC.;; CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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