Taiwan FDA registration f964e9ea0ff7a22cf88f92bc0610b61d
Timela Ratti line
TW: 提美拉拉提線
Taiwan·Risk Class 2·Fuzhan Mei Technology Co., Ltd. Dongshan Factory·Registered Dec 01, 2022 – Dec 01, 2027ActiveRegistration details
- Analysis ID
- f964e9ea0ff7a22cf88f92bc0610b61d
Company information
- Manufacturer
- Fuzhan Mei Technology Co., Ltd. Dongshan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DIAMOND BIOTECHNOLOGY 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)
- I.4840 Absorbable polydioxanone surgical joint
- Import Information
- Domestic;; Contract manufacturing;; Security surveillance
Dates and status
- Registration Date
- Dec 01, 2022
- Expiry Date
- Dec 01, 2027
About this record
Access comprehensive regulatory information for Timela Ratti line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f964e9ea0ff7a22cf88f92bc0610b61d and manufactured by Fuzhan Mei Technology Co., Ltd. Dongshan Factory. The authorized representative in Taiwan is DIAMOND BIOTECHNOLOGY CO., LTD..
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