Taiwan FDA registration 292a1201f95bdc4853032bdfe834409a
"Aegis Medical" single-use biopsy forceps
TW: “安杰思醫學”一次性使用活組織取樣鉗
Taiwan·Risk Class 2·Hangzhou AGS MedTech Co., Ltd.·Registered Apr 26, 2022 – Apr 26, 2027ActiveRegistration details
- Analysis ID
- 292a1201f95bdc4853032bdfe834409a
- Customs Code
- DHA09200131908
Company information
- Manufacturer
- Hangzhou AGS MedTech Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- KUO'S YUAN IN ENTERPRISE 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.1075 腸胃科-泌尿科生檢器械
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 26, 2022
- Expiry Date
- Apr 26, 2027
About this record
Access comprehensive regulatory information for "Aegis Medical" single-use 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 292a1201f95bdc4853032bdfe834409a and manufactured by Hangzhou AGS MedTech Co., Ltd.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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