Taiwan FDA registration 000db7fbced0789527a5c71137a3fb25
"Green Cross" single-use sterile vaginal dilator
TW: “綠十字”一次性使用無菌陰道擴張器
Taiwan·Risk Class 2·Taizhou Kangjian Medical Equipment Co., Ltd.·Registered Aug 15, 2017 – Aug 15, 2027ActiveRegistration details
- Analysis ID
- 000db7fbced0789527a5c71137a3fb25
- Customs Code
- DHA09200086402
Company information
- Manufacturer
- Taizhou Kangjian Medical Equipment Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- YIH JIANG ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.4530 婦產科專用手動器械
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Aug 15, 2017
- Expiry Date
- Aug 15, 2027
About this record
Access comprehensive regulatory information for "Green Cross" single-use sterile vaginal dilator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 000db7fbced0789527a5c71137a3fb25 and manufactured by Taizhou Kangjian Medical Equipment Co., Ltd.. The authorized representative in Taiwan is YIH JIANG ENTERPRISE CO., LTD..
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