Taiwan FDA registration f38e565236a5fae56a584a5029699463
"Lominnis" Aluma Wave Tightening System
TW: “洛明尼斯”愛露瑪電波緊膚系統
Taiwan·Risk Class 2·LUMENIS LTD.·Registered May 01, 2008 – May 01, 2013CancelledRegistration details
- Analysis ID
- f38e565236a5fae56a584a5029699463
- Customs Code
- DHA00601883505
Company information
- Manufacturer
- LUMENIS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- Taiwan Branch of Hong Kong Commercial Medical Laser Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- May 01, 2008
- Expiry Date
- May 01, 2013
- Cancellation Date
- Aug 13, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lominnis" Aluma Wave Tightening System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f38e565236a5fae56a584a5029699463 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is Taiwan Branch of Hong Kong Commercial Medical Laser Co., Ltd.
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