Taiwan FDA registration 8dfa963418c020382ac08b55f8eecf8f
"Nidek" diode laser solidifier
TW: "尼德克"二極體雷射光凝固儀
Taiwan·Risk Class 2·NIDEK CO., LTD.·Registered Apr 21, 2006 – Apr 21, 2016CancelledRegistration details
- Analysis ID
- 8dfa963418c020382ac08b55f8eecf8f
- Customs Code
- DHA00601433201
Company information
- Manufacturer
- NIDEK CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Apr 21, 2006
- Expiry Date
- Apr 21, 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" diode laser solidifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8dfa963418c020382ac08b55f8eecf8f and manufactured by NIDEK CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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