Taiwan FDA registration 8e71caa1b930084aa90890914ae76b10

"Nidek" corneal endothelial cell microscopy

TW: "尼德克"角膜內皮細胞顯微鏡
Taiwan flagTaiwan·Risk Class 2·NIDEK TECHNOLOGIES S.R.L.·Registered Jan 08, 2007 – Jan 08, 2017Cancelled
Registration details
Analysis ID
8e71caa1b930084aa90890914ae76b10
Customs Code
DHA00601765702
Company information
Manufacturer Country
Italy
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.1850 交流電力式細隙燈
Import Information
import
Dates and status
Registration Date
Jan 08, 2007
Expiry Date
Jan 08, 2017
Cancellation Date
Nov 04, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Nidek" corneal endothelial cell microscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8e71caa1b930084aa90890914ae76b10 and manufactured by NIDEK TECHNOLOGIES S.R.L.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NIDEK CO., LTD., HAMACHO PLANT, and 1 recent registrations in the same category. 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.

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