Taiwan FDA registration cc81798b0040e23b87acc04df4816c47
“NIDEK” Green Laser Photocoagulator
TW: “尼德克”雷射光凝固儀
Taiwan·Risk Class 2·MD·NIDEK CO., LTD. HAMACHO PLANT·Registered Mar 15, 2016 – Mar 15, 2026ExpiredRegistration details
- Analysis ID
- cc81798b0040e23b87acc04df4816c47
- License Form
- Ministry of Health Medical Device Import No. 028261
- Customs Code
- DHA05602826107
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)
- M4690 Ophthalmic photocoagulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 15, 2016
- Expiry Date
- Mar 15, 2026
About this record
Access comprehensive regulatory information for “NIDEK” Green Laser Photocoagulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc81798b0040e23b87acc04df4816c47 and manufactured by NIDEK CO., LTD. HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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