Taiwan FDA registration 8a387c06d796dc5408ddede2ef82de1d
"NIDEK" Perimeter (Non-sterile)
TW: "尼德克" 視野計 (未滅菌)
Taiwan·Risk Class 1·MD·NIDEK CO., LTD. HAMACHO PLANT·Registered Jun 30, 2015 – Jun 30, 2020CancelledRegistration details
- Analysis ID
- 8a387c06d796dc5408ddede2ef82de1d
- License Form
- Ministry of Health Medical Device Import No. 015397
- Customs Code
- DHA09401539705
Company information
- Manufacturer
- NIDEK CO., LTD. HAMACHO PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1605 field of view mirror
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 30, 2015
- Expiry Date
- Jun 30, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "NIDEK" Perimeter (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8a387c06d796dc5408ddede2ef82de1d and manufactured by NIDEK CO., LTD. HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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