Taiwan FDA registration 90d40a49fd9863c77ee5aad68bd7519e
"Nidek" multi-wavelength fundus photocoagulation laser
TW: “尼德克”多波長眼底光凝雷射儀
Taiwan·Risk Class 2·NIDEK CO., LTD. HAMACHO PLANT·Registered Mar 08, 2010 – Mar 08, 2015CancelledRegistration details
- Analysis ID
- 90d40a49fd9863c77ee5aad68bd7519e
- Customs Code
- DHA00602063502
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 Ophthalmology
- Product Type (Level 2)
- M.4690 眼科用光凝固儀
- Import Information
- import
Dates and status
- Registration Date
- Mar 08, 2010
- Expiry Date
- Mar 08, 2015
- Cancellation Date
- Apr 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nidek" multi-wavelength fundus photocoagulation laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 90d40a49fd9863c77ee5aad68bd7519e 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