Taiwan FDA registration a810731acf62833252b852410773dc65
"Kupo" disposable urethral guide sheath
TW: “庫珀”一次性使用輸尿管導引鞘
Taiwan·Risk Class 2·Copper Medical Technology Co., Ltd.·Registered Sep 16, 2024 – Sep 16, 2029ActiveRegistration details
- Analysis ID
- a810731acf62833252b852410773dc65
- Customs Code
- DHA09200161104
Company information
- Manufacturer
- Copper Medical Technology Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- ECOMed Biotech 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
- Sep 16, 2024
- Expiry Date
- Sep 16, 2029
About this record
Access comprehensive regulatory information for "Kupo" disposable urethral guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a810731acf62833252b852410773dc65 and manufactured by Copper Medical Technology Co., Ltd.. The authorized representative in Taiwan is ECOMed Biotech 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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