Taiwan FDA registration 2422726aef073d34271099782a725ac2
"Yobamei" Skin Irritation Bottle (Sterilized)
TW: "優百媚" 皮膚刺激瓶 (滅菌)
Taiwan·Risk Class 1·U-BIOMED INC.·Registered Dec 28, 2015 – Dec 28, 2020CancelledRegistration details
- Analysis ID
- 2422726aef073d34271099782a725ac2
- Customs Code
- DHA09401601904
Company information
- Manufacturer
- U-BIOMED INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HAO SHAN BIOTECHNOLOGY CO., LTD
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 28, 2015
- Expiry Date
- Dec 28, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Yobamei" Skin Irritation Bottle (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2422726aef073d34271099782a725ac2 and manufactured by U-BIOMED INC.. The authorized representative in Taiwan is HAO SHAN BIOTECHNOLOGY CO., LTD.
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