Taiwan FDA registration a6008231fcecc50d59fc6ccd861c961c
"Lomenis" pulsed light/laser and its accessories
TW: "洛明尼斯"脈衝光/雷射儀及其配件
Taiwan·Risk Class 2·LUMENIS LTD.·Registered Aug 23, 2006 – Aug 23, 2011CancelledRegistration details
- Analysis ID
- a6008231fcecc50d59fc6ccd861c961c
- Customs Code
- DHA00601702902
Company information
- Manufacturer
- LUMENIS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- MOSTYLE CORPORATION
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.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Aug 23, 2006
- Expiry Date
- Aug 23, 2011
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lomenis" pulsed light/laser and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a6008231fcecc50d59fc6ccd861c961c and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is MOSTYLE CORPORATION.
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