Taiwan FDA registration c23a49fa2c06fa841ed83f56f430731a
"Nidek" ophthalmic optical tomography
TW: “尼德克”眼用光學斷層掃描儀
Taiwan·Risk Class 2·NIDEK CO., LTD. HAMACHO PLANT·Registered Mar 12, 2010 – Mar 12, 2030ActiveRegistration details
- Analysis ID
- c23a49fa2c06fa841ed83f56f430731a
- Customs Code
- DHA00602066307
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. Performance changes (model: RS-3000 Advance): As detailed in Chinese copy of the copy.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1570 Fundus Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Mar 12, 2010
- Expiry Date
- Mar 12, 2030
About this record
Access comprehensive regulatory information for "Nidek" ophthalmic optical tomography in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c23a49fa2c06fa841ed83f56f430731a and manufactured by NIDEK CO., LTD. HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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