Taiwan FDA registration daecc10479ea4b266ac48b2a898b97d3
“Pollogen” DIVINE Pro System
TW: “博樂金”德邁電波除皺系統
Taiwan·Risk Class 2·MD·Pollogen Ltd.·Registered Nov 22, 2021 – Nov 22, 2026ActiveRegistration details
- Analysis ID
- daecc10479ea4b266ac48b2a898b97d3
- License Form
- Ministry of Health Medical Device Import No. 035065
- Customs Code
- DHA05603506501
Company information
- Manufacturer
- Pollogen Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch
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)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 22, 2021
- Expiry Date
- Nov 22, 2026
About this record
Access comprehensive regulatory information for “Pollogen” DIVINE Pro System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number daecc10479ea4b266ac48b2a898b97d3 and manufactured by Pollogen Ltd.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
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