Taiwan FDA registration a871fb257441899af700cb26e99c3ddd
“Lumenis” OtoLase System
TW: “洛明尼斯”歐特雷系統
Taiwan·Risk Class 2·MD·LUMENIS LTD.·Registered Mar 05, 2018 – Mar 05, 2028ActiveRegistration details
- Analysis ID
- a871fb257441899af700cb26e99c3ddd
- License Form
- Ministry of Health Medical Device Import No. 030947
- Customs Code
- DHA05603094707
Company information
- Manufacturer
- LUMENIS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- BOSTON SCIENTIFIC INTERNATIONAL B.V., TAIWAN BRANCH (NETHERLANDS)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 05, 2018
- Expiry Date
- Mar 05, 2028
About this record
Access comprehensive regulatory information for “Lumenis” OtoLase System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a871fb257441899af700cb26e99c3ddd and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is BOSTON SCIENTIFIC INTERNATIONAL B.V., TAIWAN BRANCH (NETHERLANDS).
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