Taiwan FDA registration b90bf7da3a4cf997faa51c9a8751b428
“Pollogen” gene O+ RF Skin Treatment System
TW: “博樂晶”勁歐電波除皺系統
Taiwan·Risk Class 2·MD·Pollogen Ltd.·Registered Dec 19, 2014 – Dec 19, 2024ExpiredRegistration details
- Analysis ID
- b90bf7da3a4cf997faa51c9a8751b428
- License Form
- Ministry of Health Medical Device Import No. 026869
- Customs Code
- DHA05602686901
Company information
- Manufacturer
- Pollogen Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 19, 2014
- Expiry Date
- Dec 19, 2024
About this record
Access comprehensive regulatory information for “Pollogen” gene O+ RF Skin Treatment System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b90bf7da3a4cf997faa51c9a8751b428 and manufactured by Pollogen Ltd.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
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