Taiwan FDA registration 213da321fb1db3ea6f931ca218fed020
“BabySoothe” Dermatological Gel
TW: “貝比欣”凝膠
Taiwan·Risk Class 2·MD·Oculus Technologies of Mexico, S.A. de C.V.·Registered Dec 30, 2022 – Dec 30, 2027ActiveRegistration details
- Analysis ID
- 213da321fb1db3ea6f931ca218fed020
- License Form
- Ministry of Health Medical Device Import No. 036150
- Customs Code
- DHA05603615007
Company information
- Manufacturer
- Oculus Technologies of Mexico, S.A. de C.V.
- Manufacturer Country
- Mexico
- Authorized Representative
- CHIAEN PHARMACEUTICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4022 Waterborne wound and burn coverings
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 30, 2022
- Expiry Date
- Dec 30, 2027
About this record
Access comprehensive regulatory information for “BabySoothe” Dermatological Gel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 213da321fb1db3ea6f931ca218fed020 and manufactured by Oculus Technologies of Mexico, S.A. de C.V.. The authorized representative in Taiwan is CHIAEN PHARMACEUTICAL CO., LTD..
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