Taiwan FDA registration 76ce802d27ff981c07e4bae90459861e
"Lominnis" Laixin diode laser system
TW: “洛明尼斯”萊新二極體雷射系統
Taiwan·Risk Class 2·LUMENIS INC.;; RH USA INC.·Registered Jul 19, 2010 – Jul 19, 2015CancelledRegistration details
- Analysis ID
- 76ce802d27ff981c07e4bae90459861e
- Customs Code
- DHA00602126003
Company information
- Manufacturer
- LUMENIS INC.;; RH USA INC.
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Branch of Hong Kong Commercial Medical Laser Co., Ltd
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
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Jul 19, 2010
- Expiry Date
- Jul 19, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Lominnis" Laixin diode 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 76ce802d27ff981c07e4bae90459861e and manufactured by LUMENIS INC.;; RH USA INC.. The authorized representative in Taiwan is Taiwan Branch of Hong Kong Commercial Medical Laser Co., Ltd.
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