Taiwan FDA registration 1dd49f4df13accb00d0e792f29fa4a26
“Mediland” QuadLED Surgical Light
TW: “鼎眾”外科手術燈
Taiwan·Risk Class 2·MD·Dingzhong Co., Ltd. Linkou Factory·Registered Mar 29, 2023 – Mar 29, 2028ActiveRegistration details
- Analysis ID
- 1dd49f4df13accb00d0e792f29fa4a26
- License Form
- Ministry of Health Medical Device Manufacturing No. 007750
Company information
- Manufacturer
- Dingzhong Co., Ltd. Linkou Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Dingzhong Co., Ltd. Linkou Factory
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)
- I4580 Surgical light
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 29, 2023
- Expiry Date
- Mar 29, 2028
About this record
Access comprehensive regulatory information for “Mediland” QuadLED 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 1dd49f4df13accb00d0e792f29fa4a26 and manufactured by Dingzhong Co., Ltd. Linkou Factory. The authorized representative in Taiwan is Dingzhong Co., Ltd. Linkou Factory.
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