Taiwan FDA registration f50317d71721b13bd76dd428f359947d
"Boston Tech" symmetrical balloon expansion catheter
TW: “波士頓科技”對稱式氣球擴張導管
Registration details
- Analysis ID
- f50317d71721b13bd76dd428f359947d
- Customs Code
- DHA00602048700
Company information
- Manufacturer
- Boston Scientific Limited
- Manufacturer Country
- Ireland
- Authorized Representative
- Dutch Boston Technology Co., Ltd. Taiwan Branch
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Dec 15, 2009
- Expiry Date
- Dec 15, 2024
- Cancellation Date
- Mar 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Boston Tech" symmetrical balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f50317d71721b13bd76dd428f359947d and manufactured by Boston Scientific Limited. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.
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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