Taiwan FDA registration 6209059afda02044d0217ed737dac92b
“NIDEK” Microperimeter
TW: “尼德克”微視野計
Taiwan·Risk Class 2·MD·NIDEK CO., LTD. HAMACHO PLANT·Registered Nov 27, 2015 – Nov 27, 2025ExpiredRegistration details
- Analysis ID
- 6209059afda02044d0217ed737dac92b
- License Form
- Ministry of Health Medical Device Import No. 027862
- Customs Code
- DHA05602786202
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
- Nov 27, 2015
- Expiry Date
- Nov 27, 2025
About this record
Access comprehensive regulatory information for “NIDEK” Microperimeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6209059afda02044d0217ed737dac92b and manufactured by NIDEK CO., LTD. HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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