Taiwan FDA registration 958de0c647a8a11586b1a4aa51a96584
"Disien" dental surgical light (unsterilized)
TW: "迪西安"牙科用手術燈(未滅菌)
Taiwan·Risk Class 1·DCI EQUIPMENT·Registered Mar 26, 2013 – Mar 26, 2018CancelledRegistration details
- Analysis ID
- 958de0c647a8a11586b1a4aa51a96584
- Customs Code
- DHA04401284307
Company information
- Manufacturer
- DCI EQUIPMENT
- Manufacturer Country
- United States
- Authorized Representative
- MYWAY INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Equipment "Dental Surgical Light (F.4630)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4630 牙科用手術燈
- Import Information
- import
Dates and status
- Registration Date
- Mar 26, 2013
- Expiry Date
- Mar 26, 2018
- Cancellation Date
- Nov 26, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Disien" dental surgical light (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 958de0c647a8a11586b1a4aa51a96584 and manufactured by DCI EQUIPMENT. The authorized representative in Taiwan is MYWAY INTERNATIONAL CO., LTD..
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