Taiwan FDA registration 68b8ce9fc9cfb41ac0d40e3673d874b0
"Morning Yang" battery-operated translucent (unsterilized)
TW: “朝揚”電池式透照器(未滅菌)
Taiwan·Risk Class 1·Chaoyang Plastic Factory Co., Ltd·Registered Jan 18, 2008 – Jan 18, 2028ActiveRegistration details
- Analysis ID
- 68b8ce9fc9cfb41ac0d40e3673d874b0
Company information
- Manufacturer
- Chaoyang Plastic Factory Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Chaoyang Plastic Factory Co., Ltd
Product details
- Intended Use
- It is limited to the first level of identification scope of the "Transilluminator (M.1945)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1945 Transilluminator
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 18, 2008
- Expiry Date
- Jan 18, 2028
About this record
Access comprehensive regulatory information for "Morning Yang" battery-operated translucent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 68b8ce9fc9cfb41ac0d40e3673d874b0 and manufactured by Chaoyang Plastic Factory Co., Ltd. The authorized representative in Taiwan is Chaoyang Plastic Factory Co., Ltd.
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