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“NIDEK” Laser Speckle Flowgraphy - Taiwan Registration 7e4608c17768f0b36dfdd97a4b1f34f7

Access comprehensive regulatory information for “NIDEK” Laser Speckle Flowgraphy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e4608c17768f0b36dfdd97a4b1f34f7 and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

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7e4608c17768f0b36dfdd97a4b1f34f7
Registration Details
Taiwan FDA Registration: 7e4608c17768f0b36dfdd97a4b1f34f7
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Device Details

“NIDEK” Laser Speckle Flowgraphy
TW: “尼德克”雷射光斑血流造影儀
Risk Class 2
MD

Registration Details

7e4608c17768f0b36dfdd97a4b1f34f7

Ministry of Health Medical Device Import No. 033201

DHA05603320109

Company Information

Product Details

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

M Ophthalmic devices

M1570 fundus mirror

Imported from abroad

Dates and Status

Jan 10, 2020

Jan 10, 2025