Taiwan FDA registration e719c9850bafba8d2ae2327038b78388
"Nidek" micro-field meter
TW: "尼德克"微視野計
Taiwan·Risk Class 2·NIDEK TECHNOLOGIES S.R.L.·Registered Sep 15, 2006 – Sep 15, 2016CancelledRegistration details
- Analysis ID
- e719c9850bafba8d2ae2327038b78388
- Customs Code
- DHA00601711202
Company information
- Manufacturer
- NIDEK TECHNOLOGIES S.R.L.
- Manufacturer Country
- Italy
- 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
- Product Type (Level 2)
- M.1780 Retinal Lens
- Import Information
- import
Dates and status
- Registration Date
- Sep 15, 2006
- Expiry Date
- Sep 15, 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" micro-field meter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e719c9850bafba8d2ae2327038b78388 and manufactured by NIDEK TECHNOLOGIES S.R.L.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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