Taiwan FDA registration 9f6eeff6f43105e17887547f0d7d70a8
"Shangxian" disposable biopsy forceps
TW: “尚賢”一次性活檢鉗
Taiwan·Risk Class 2·Shangxian Minimal Invasive Inc.·Registered Feb 03, 2021 – Feb 03, 2026ExpiredRegistration details
- Analysis ID
- 9f6eeff6f43105e17887547f0d7d70a8
- Customs Code
- DHA09200121101
Company information
- Manufacturer
- Shangxian Minimal Invasive Inc.
- Manufacturer Country
- China
- Authorized Representative
- WELMORE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Feb 03, 2021
- Expiry Date
- Feb 03, 2026
About this record
Access comprehensive regulatory information for "Shangxian" disposable biopsy forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9f6eeff6f43105e17887547f0d7d70a8 and manufactured by Shangxian Minimal Invasive Inc.. The authorized representative in Taiwan is WELMORE CO., LTD..
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