Taiwan FDA registration 72839e0986cd29ed80ae820579db59dc
"Wonderrhenium" light source system
TW: “旺德錸”光源系統
Taiwan·Risk Class 2·BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory·Registered Jul 04, 2022 – Jul 04, 2027ActiveRegistration details
- Analysis ID
- 72839e0986cd29ed80ae820579db59dc
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Guangyan Biomedical Technology Co., Ltd
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jul 04, 2022
- Expiry Date
- Jul 04, 2027
About this record
Access comprehensive regulatory information for "Wonderrhenium" light source system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72839e0986cd29ed80ae820579db59dc and manufactured by BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory. The authorized representative in Taiwan is Guangyan Biomedical Technology 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