Taiwan FDA registration bfb35e0ede95dd2da76b0acf98ac134a

"Nidek" mydriatic automatic fundus camera

TW: “尼德克”免散瞳自動眼底照相機
Taiwan flagTaiwan·Risk Class 2·NIDEK CO., LTD.;; Taishodo Vietnam Company Limited·Registered Aug 15, 2007 – Aug 15, 2022Cancelled
Registration details
Analysis ID
bfb35e0ede95dd2da76b0acf98ac134a
Customs Code
DHA00601820501
Company information
Manufacturer Country
Viet Nam;;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.1120 Ophthalmic camera
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Aug 15, 2007
Expiry Date
Aug 15, 2022
Cancellation Date
Apr 12, 2024
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" mydriatic automatic fundus camera in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bfb35e0ede95dd2da76b0acf98ac134a and manufactured by NIDEK CO., LTD.;; Taishodo Vietnam Company Limited. 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 Taishodo Vietnam Company Limited;; NIDEK CO., LTD., 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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