Taiwan FDA registration 7e4608c17768f0b36dfdd97a4b1f34f7
“NIDEK” Laser Speckle Flowgraphy
TW: “尼德克”雷射光斑血流造影儀
Taiwan·Risk Class 2·MD·NIDEK CO., LTD., HAMACHO PLANT·Registered Jan 10, 2020 – Jan 10, 2025ExpiredRegistration details
- Analysis ID
- 7e4608c17768f0b36dfdd97a4b1f34f7
- License Form
- Ministry of Health Medical Device Import No. 033201
- Customs Code
- DHA05603320109
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)
- M1570 fundus mirror
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 10, 2020
- Expiry Date
- Jan 10, 2025
About this record
Access comprehensive regulatory information for “NIDEK” Laser Speckle Flowgraphy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e4608c17768f0b36dfdd97a4b1f34f7 and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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