Taiwan FDA registration e14eda7dab0494e29481ad64e9ae0bb3
"Weili" urinary tract with guidewire
TW: “維力”泌尿道用導絲
Taiwan·Risk Class 2·Well Lead Medical Co., Ltd.·Registered Mar 25, 2022 – Mar 25, 2027ActiveRegistration details
- Analysis ID
- e14eda7dab0494e29481ad64e9ae0bb3
- Customs Code
- DHA09200131401
Company information
- Manufacturer
- Well Lead Medical Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- Kang Cheng Medical Technology Co., Ltd
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5130 泌尿導管及其附件
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 25, 2022
- Expiry Date
- Mar 25, 2027
About this record
Access comprehensive regulatory information for "Weili" urinary tract with guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e14eda7dab0494e29481ad64e9ae0bb3 and manufactured by Well Lead Medical Co., Ltd.. The authorized representative in Taiwan is Kang Cheng Medical Technology Co., Ltd.
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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