Taiwan FDA registration e9d1aa4145af7d5e8a47386d92598e48
"Nidek" ophthalmic refractive machine (unsterilized)
TW: "尼德克" 眼科驗光機(未滅菌)
Taiwan·Risk Class 1·NIDEK CO., LTD. HAMACHO PLANT·Registered Mar 04, 2011 – Mar 04, 2026CancelledRegistration details
- Analysis ID
- e9d1aa4145af7d5e8a47386d92598e48
- Customs Code
- DHA04400997909
Company information
- Manufacturer
- NIDEK CO., LTD. HAMACHO PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of ophthalmic optometry machine (M.1760) of the management measures for medical equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1760 Automatic Ophthalmic Optical Machine
- Import Information
- import
Dates and status
- Registration Date
- Mar 04, 2011
- Expiry Date
- Mar 04, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Nidek" ophthalmic refractive machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e9d1aa4145af7d5e8a47386d92598e48 and manufactured by NIDEK CO., LTD. HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices