Taiwan FDA registration 158588514bcdd99a3be63191fa550bdc
"Mindray" diode surgical light
TW: “邁瑞”二極體手術燈
Registration details
- Analysis ID
- 158588514bcdd99a3be63191fa550bdc
- Customs Code
- DHA09200116201
Company information
- Manufacturer Country
- China
- Authorized Representative
- SOAR INSTRUMENT-TECH. 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.4580 Surgical lamp
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jun 16, 2020
- Expiry Date
- Jun 16, 2025
About this record
Access comprehensive regulatory information for "Mindray" diode surgical light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 158588514bcdd99a3be63191fa550bdc and manufactured by Nanjing Mindray Bio-Medical Electronics CO., Ltd.. The authorized representative in Taiwan is SOAR INSTRUMENT-TECH. 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