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"Heidelberg" cataract and refractive imaging diagnostic platform - Taiwan Registration bee3a47029d19974bf164bdc4c8ae9c0

Access comprehensive regulatory information for "Heidelberg" cataract and refractive imaging diagnostic platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bee3a47029d19974bf164bdc4c8ae9c0 and manufactured by HEIDELBERG ENGINEERING GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..

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bee3a47029d19974bf164bdc4c8ae9c0
Registration Details
Taiwan FDA Registration: bee3a47029d19974bf164bdc4c8ae9c0
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Device Details

"Heidelberg" cataract and refractive imaging diagnostic platform
TW: โ€œๆตทๅพทๅ กโ€็™ฝๅ…ง้šœๅŠๅฑˆๅ…‰ๅฝฑๅƒ่จบๆ–ทๅนณๅฐ
Risk Class 2

Registration Details

bee3a47029d19974bf164bdc4c8ae9c0

DHA05603291007

Company Information

Germany

Product Details

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

M Ophthalmology

M.1570 Fundus Mirrors

import

Dates and Status

Oct 31, 2019

Oct 31, 2029