Taiwan FDA registration bbb940e706a9243c60e2d47c124c98fa
"NIDEK" Tabletop Refraction System (Non-Sterile)
TW: "尼德克"桌上型屈光系統(未滅菌)
Taiwan·Risk Class 1·MD·NIDEK CO., LTD., HAMACHO PLANT·Registered Oct 13, 2017 – Oct 13, 2022CancelledRegistration details
- Analysis ID
- bbb940e706a9243c60e2d47c124c98fa
- License Form
- Ministry of Health Medical Device Import No. 018401
- Customs Code
- DHA09401840101
Company information
- Manufacturer
- NIDEK CO., LTD., HAMACHO PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1760 Ophthalmic Refractive Machine
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 13, 2017
- Expiry Date
- Oct 13, 2022
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "NIDEK" Tabletop Refraction System (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bbb940e706a9243c60e2d47c124c98fa and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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