Taiwan FDA registration f8a9b5d2f931c6b933f6ff5625218d30
"Lominnis" pulsed illumination / rubidium Yak / diode laser system
TW: “洛明尼斯”脈衝式光照/ 銣雅克/ 二極體雷射系統
Taiwan·Risk Class 2·LUMENIS LTD.·Registered Jun 02, 2008 – Jun 02, 2018CancelledRegistration details
- Analysis ID
- f8a9b5d2f931c6b933f6ff5625218d30
- Customs Code
- DHA00601888303
Company information
- Manufacturer
- LUMENIS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- LUMENIS (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, 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
- Jun 02, 2008
- Expiry Date
- Jun 02, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lominnis" pulsed illumination / rubidium Yak / diode laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f8a9b5d2f931c6b933f6ff5625218d30 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is LUMENIS (HK) LIMITED TAIWAN BRANCH.
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