Taiwan FDA registration 9ddf1f165f032c7fa97679b5a6d504b6
"Yousjiai" endoscopic surgery platform
TW: “優思吉愛”內視鏡手術平台
Taiwan·Risk Class 2·USGI Medical·Registered Oct 28, 2024 – Oct 28, 2029ActiveRegistration details
- Analysis ID
- 9ddf1f165f032c7fa97679b5a6d504b6
- Customs Code
- DHA05603763602
Company information
- Manufacturer
- USGI Medical
- Manufacturer Country
- United States
- Authorized Representative
- AP Biotech 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.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Oct 28, 2024
- Expiry Date
- Oct 28, 2029
About this record
Access comprehensive regulatory information for "Yousjiai" endoscopic surgery platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ddf1f165f032c7fa97679b5a6d504b6 and manufactured by USGI Medical. The authorized representative in Taiwan is AP Biotech 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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