Taiwan FDA registration 8f309d74cf22d9a246730294645ebeed
“Nidek” Auto Ref/Kerato/ Tono/Pachymeter
TW: “尼德克”全自動驗光/角膜曲率/眼壓/角膜厚度測量儀
Taiwan·Risk Class 2·MD·NIDEK CO., LTD., HAMACHO PLANT·Registered Sep 01, 2016 – Sep 01, 2026ActiveRegistration details
- Analysis ID
- 8f309d74cf22d9a246730294645ebeed
- License Form
- Ministry of Health Medical Device Import No. 028774
- Customs Code
- DHA05602877400
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 Ophthalmic devices
- Product Type (Level 2)
- M1930 Tonometer and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 01, 2016
- Expiry Date
- Sep 01, 2026
About this record
Access comprehensive regulatory information for “Nidek” Auto Ref/Kerato/ Tono/Pachymeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f309d74cf22d9a246730294645ebeed and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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