Taiwan FDA registration 50096fdc35785481ec6a6493c1af9e93
“NIDEK” Ophthalmic YAG Laser System
TW: “尼德克”眼科雅各雷射系統
Taiwan·Risk Class 2·MD·NIDEK CO., LTD. HAMACHO PLANT·Registered Oct 04, 2019 – Oct 04, 2024ExpiredRegistration details
- Analysis ID
- 50096fdc35785481ec6a6493c1af9e93
- License Form
- Ministry of Health Medical Device Import No. 032888
- Customs Code
- DHA05603288801
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)
- M4392 Posterior capsulectomy with Nd:YAG laser
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 04, 2019
- Expiry Date
- Oct 04, 2024
About this record
Access comprehensive regulatory information for “NIDEK” Ophthalmic YAG Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50096fdc35785481ec6a6493c1af9e93 and manufactured by NIDEK CO., LTD. HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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