Taiwan FDA registration 94058e2a4d60232b4784fc7100bc5eb0
"Nidek" digital corner mirror
TW: “尼德克”數位隅角鏡
Taiwan·Risk Class 2·NIDEK CO., LTD., HAMACHO PLANT·Registered Mar 16, 2020 – Mar 16, 2030ActiveRegistration details
- Analysis ID
- 94058e2a4d60232b4784fc7100bc5eb0
- Customs Code
- DHA05603332106
Company information
- Manufacturer
- NIDEK CO., LTD., HAMACHO PLANT
- 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
- Product Type (Level 2)
- M.1120 ophthalmic camera;; M.1660 boresight angle prism
- Import Information
- import
Dates and status
- Registration Date
- Mar 16, 2020
- Expiry Date
- Mar 16, 2030
About this record
Access comprehensive regulatory information for "Nidek" digital corner mirror in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94058e2a4d60232b4784fc7100bc5eb0 and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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