Taiwan FDA registration 9f95b1a4d78beb7e65461498ecf3b85f
Niedek corneal radius measuring device
TW: 尼德克角膜半徑測量裝置
Taiwan·Risk Class 1·NIDEK CO., LTD.·Registered Apr 15, 2006 – Apr 15, 2011CancelledRegistration details
- Analysis ID
- 9f95b1a4d78beb7e65461498ecf3b85f
- Customs Code
- DHA04400392801
Company information
- Manufacturer
- NIDEK CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Emperor Prayer Limited
Product details
- Intended Use
- It is limited to the first level of identification of the "Corneal Radius Measurement Device (M.1450)" of the Medical Device Management Regulations.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1450 角膜弧度量測器
- Import Information
- import
Dates and status
- Registration Date
- Apr 15, 2006
- Expiry Date
- Apr 15, 2011
- Cancellation Date
- Aug 11, 2006
Cancellation information
- Status
- Logged out
- Reason
- 依藥事法第97條規定
About this record
Access comprehensive regulatory information for Niedek corneal radius measuring device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f95b1a4d78beb7e65461498ecf3b85f and manufactured by NIDEK CO., LTD.. The authorized representative in Taiwan is Emperor Prayer Limited.
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