Taiwan FDA registration 368697082e87e528f632ece58b17c468
"Nidek" corneal lamellar knife (unsterilized)
TW: "尼德克" 角膜板層刀 (未滅菌)
Taiwan·Risk Class 1·NIDEK CO., LTD., HAMACHO PLANT·Registered Aug 01, 2011 – Aug 01, 2016CancelledRegistration details
- Analysis ID
- 368697082e87e528f632ece58b17c468
- Customs Code
- DHA04401066206
Company information
- Manufacturer
- NIDEK CO., LTD., HAMACHO PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "corneal knife (M.4370)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4370 Corneal knife
- Import Information
- import
Dates and status
- Registration Date
- Aug 01, 2011
- Expiry Date
- Aug 01, 2016
- Cancellation Date
- Apr 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nidek" corneal lamellar knife (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 368697082e87e528f632ece58b17c468 and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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