Taiwan FDA registration d1eb2f97bb5beedbab59475e44a9e7bb
"Lominnis" Seri multi-eye laser and its accessories
TW: “洛明尼斯”色麗多眼用雷射儀及其配件
Taiwan·Risk Class 2·Lumenis Be Inc.·Registered Jul 09, 2009 – Jul 09, 2029ActiveRegistration details
- Analysis ID
- d1eb2f97bb5beedbab59475e44a9e7bb
- Customs Code
- DHA00602004800
Company information
- Manufacturer
- Lumenis Be Inc.
- Manufacturer Country
- United States
- 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)
- M Ophthalmology
- Product Type (Level 2)
- M.4390 眼科雷射裝置
- Import Information
- import
Dates and status
- Registration Date
- Jul 09, 2009
- Expiry Date
- Jul 09, 2029
About this record
Access comprehensive regulatory information for "Lominnis" Seri multi-eye 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 d1eb2f97bb5beedbab59475e44a9e7bb and manufactured by Lumenis Be Inc.. 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