Taiwan FDA registration 56d6c011dcb6b098c84c3a654f80b222

"Nidek" corneal endothelial cell microscopy

TW: “尼德克”角膜內皮細胞顯微鏡
Taiwan flagTaiwan·Risk Class 2·NIDEK CO., LTD., HAMACHO PLANT·Registered Jan 09, 2013 – Jan 09, 2028Active
Registration details
Analysis ID
56d6c011dcb6b098c84c3a654f80b222
Customs Code
DHA00602442702
Company information
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.1570 Fundus Mirrors
Import Information
import
Dates and status
Registration Date
Jan 09, 2013
Expiry Date
Jan 09, 2028
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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 56d6c011dcb6b098c84c3a654f80b222 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, 1 companies making similar products including NIDEK TECHNOLOGIES S.R.L., 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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