Taiwan FDA registration dfc06d0a8b88e9c284c8a1629a2028c7
"BOTTEN" dental surgery light (unsterilized)
TW: "博騰"牙科手術燈(未滅菌)
Taiwan·Risk Class 1·BURTON MEDICAL PRODUCTS CORPORATION·Registered May 20, 2011 – May 20, 2016CancelledRegistration details
- Analysis ID
- dfc06d0a8b88e9c284c8a1629a2028c7
- Customs Code
- DHA04401038009
Company information
- Manufacturer
- BURTON MEDICAL PRODUCTS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- KINGJING 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
- May 20, 2011
- Expiry Date
- May 20, 2016
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "BOTTEN" dental surgery 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 dfc06d0a8b88e9c284c8a1629a2028c7 and manufactured by BURTON MEDICAL PRODUCTS CORPORATION. The authorized representative in Taiwan is KINGJING INTERNATIONAL CO., LTD..
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