Taiwan FDA registration 9df877fb9602117c50fadceed9bd7442
"Laide" Westeron optical fiber dental light source and accessories (unsterilized)
TW: “來德”威士能光纖維牙科用光源及附件(未滅菌)
Taiwan·Risk Class 1·LED DENTAL INC.·Registered Feb 22, 2008 – Feb 22, 2018CancelledRegistration details
- Analysis ID
- 9df877fb9602117c50fadceed9bd7442
- Customs Code
- DHA04400653306
Company information
- Manufacturer
- LED DENTAL INC.
- Manufacturer Country
- Canada
- Authorized Representative
- Yuanhong Instrument Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Light Source for Optical Fiber Dentistry (F.4620)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4620 Light source for optical fiber dentistry
- Import Information
- import
Dates and status
- Registration Date
- Feb 22, 2008
- Expiry Date
- Feb 22, 2018
- Cancellation Date
- May 09, 2016
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Laide" Westeron optical fiber dental light source and accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9df877fb9602117c50fadceed9bd7442 and manufactured by LED DENTAL INC.. The authorized representative in Taiwan is Yuanhong Instrument Co., Ltd.
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