Taiwan FDA registration 0a4001c9f1735e8c052a759ce07d0835
"Boston Tech" Silkfrey Wire
TW: “波士頓科技”絲佛瑞導線
Taiwan·Risk Class 2·Lake Region Medical·Registered Jan 28, 2015 – Jan 28, 2030ActiveRegistration details
- Analysis ID
- 0a4001c9f1735e8c052a759ce07d0835
- Customs Code
- DHA05602695902
Company information
- Manufacturer
- Lake Region Medical
- Manufacturer Country
- United States
- 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.1330 Catheter Guide Wires
- Import Information
- import
Dates and status
- Registration Date
- Jan 28, 2015
- Expiry Date
- Jan 28, 2030
About this record
Access comprehensive regulatory information for "Boston Tech" Silkfrey Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a4001c9f1735e8c052a759ce07d0835 and manufactured by Lake Region Medical. 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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