Taiwan FDA registration ec972d7a96c5e946cbfeaecec8f4670a
"Nidek" fundus camera
TW: “尼德克”眼底照相機
Taiwan·Risk Class 2·NIDEK TECHNOLOGIES S.R.L.·Registered Aug 24, 2007 – Aug 24, 2012CancelledRegistration details
- Analysis ID
- ec972d7a96c5e946cbfeaecec8f4670a
- Customs Code
- DHA00601821501
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.1120 Ophthalmic camera
- Import Information
- import
Dates and status
- Registration Date
- Aug 24, 2007
- Expiry Date
- Aug 24, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nidek" fundus camera in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec972d7a96c5e946cbfeaecec8f4670a and manufactured by NIDEK TECHNOLOGIES S.R.L.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices