Taiwan FDA registration 52e0afa06aecb117752cca73426eb5d8
“NIDEK” Yellow Laser Photocoagulator
TW: “尼德克”黃光雷射凝固儀
Taiwan·Risk Class 2·MD·NIDEK CO., LTD., HAMACHO PLANT·Registered Sep 12, 2017 – Sep 12, 2027ActiveRegistration details
- Analysis ID
- 52e0afa06aecb117752cca73426eb5d8
- License Form
- Ministry of Health Medical Device Import No. 030190
- Customs Code
- DHA05603019002
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
- Sep 12, 2017
- Expiry Date
- Sep 12, 2027
About this record
Access comprehensive regulatory information for “NIDEK” Yellow 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 52e0afa06aecb117752cca73426eb5d8 and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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