Taiwan FDA registration 0d5ef6eb7f53bdb2900586d379a9c877
"Lominnis" Lescher's diode-removing laser system and its accessories
TW: “洛明尼斯”萊雪彗除二極體雷射系統及其附件
Taiwan·Risk Class 2·LUMENIS LTD.·Registered Jan 24, 2022 – Jan 24, 2027ActiveRegistration details
- Analysis ID
- 0d5ef6eb7f53bdb2900586d379a9c877
- Customs Code
- DHA05603519906
Company information
- Manufacturer
- LUMENIS 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)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Jan 24, 2022
- Expiry Date
- Jan 24, 2027
About this record
Access comprehensive regulatory information for "Lominnis" Lescher's diode-removing laser system 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 0d5ef6eb7f53bdb2900586d379a9c877 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
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