Taiwan FDA registration 3558a74c01ca16ae1ce7323821766614
"Lominnis" WiseVision laser indirect fundus lens
TW: “洛明尼斯”慧視雷射間接眼底鏡
Taiwan·Risk Class 2·Lumenis Be Inc.;; KEELER LTD.·Registered Aug 08, 2019 – Aug 08, 2029ActiveRegistration details
- Analysis ID
- 3558a74c01ca16ae1ce7323821766614
- Customs Code
- DHA05603278300
Company information
- Manufacturer
- Lumenis Be Inc.;; KEELER LTD.
- Manufacturer Country
- United Kingdom;;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.1570 Fundus Mirrors
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Aug 08, 2019
- Expiry Date
- Aug 08, 2029
About this record
Access comprehensive regulatory information for "Lominnis" WiseVision laser indirect fundus lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3558a74c01ca16ae1ce7323821766614 and manufactured by Lumenis Be Inc.;; KEELER LTD.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
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