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"Nidek" mydriatic automatic fundus camera - Taiwan Registration bfb35e0ede95dd2da76b0acf98ac134a

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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bfb35e0ede95dd2da76b0acf98ac134a
Registration Details
Taiwan FDA Registration: bfb35e0ede95dd2da76b0acf98ac134a
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Device Details

"Nidek" mydriatic automatic fundus camera
TW: โ€œๅฐผๅพทๅ…‹โ€ๅ…ๆ•ฃ็žณ่‡ชๅ‹•็œผๅบ•็…ง็›ธๆฉŸ
Risk Class 2
Cancelled

Registration Details

bfb35e0ede95dd2da76b0acf98ac134a

DHA00601820501

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.1120 Ophthalmic camera

Input;; Contract manufacturing

Dates and Status

Aug 15, 2007

Aug 15, 2022

Apr 12, 2024

Cancellation Information

Logged out

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