Taiwan FDA registration e28f2508cb0e55284ac52982b88f951a
"Boston Tech" urology guide steel wire
TW: "波士頓科技" 泌尿科引導鋼線
Taiwan·Risk Class 2·Lake Region Medical Limited·Registered Mar 17, 2006 – Mar 17, 2026ExpiredRegistration details
- Analysis ID
- e28f2508cb0e55284ac52982b88f951a
- Customs Code
- DHA00601416403
Company information
- Manufacturer
- Lake Region Medical 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)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Mar 17, 2006
- Expiry Date
- Mar 17, 2026
About this record
Access comprehensive regulatory information for "Boston Tech" urology guide steel wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e28f2508cb0e55284ac52982b88f951a and manufactured by Lake Region Medical 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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