Taiwan FDA registration 47859039070c38ef6004ecda9b37ec70
"Nidek" digital fundus scanner
TW: “尼德克”數位眼底掃描儀
Taiwan·Risk Class 2·NIDEK CO., LTD. HAMACHO PLANT·Registered Oct 01, 2009 – Oct 01, 2029ActiveRegistration details
- Analysis ID
- 47859039070c38ef6004ecda9b37ec70
- Customs Code
- DHA00602021506
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.1570 Fundus Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2009
- Expiry Date
- Oct 01, 2029
About this record
Access comprehensive regulatory information for "Nidek" digital fundus scanner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 47859039070c38ef6004ecda9b37ec70 and manufactured by NIDEK CO., LTD. HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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