Taiwan FDA registration 0e93544f3723ccb64a0af14eb2d78c18
"Lominnis" pulsed illumination/rubidium Jacques laser system
TW: “洛明尼斯”脈衝式光照/銣雅克雷射系統
Taiwan·Risk Class 2·LUMENIS LTD.·Registered Jun 24, 2010 – Jun 24, 2025ExpiredRegistration details
- Analysis ID
- 0e93544f3723ccb64a0af14eb2d78c18
- Customs Code
- DHA00602116407
Company information
- Manufacturer
- LUMENIS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- (Hong Kong) Lumenis Be (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 24, 2010
- Expiry Date
- Jun 24, 2025
About this record
Access comprehensive regulatory information for "Lominnis" pulsed illumination/rubidium Jacques 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 0e93544f3723ccb64a0af14eb2d78c18 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices