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"Helin" direct fundus lens and accessories - Taiwan Registration 2aa44d317f1cd11f8ba12d3e1547a9f1

Access comprehensive regulatory information for "Helin" direct fundus lens and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2aa44d317f1cd11f8ba12d3e1547a9f1 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM CO., LTD..

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2aa44d317f1cd11f8ba12d3e1547a9f1
Registration Details
Taiwan FDA Registration: 2aa44d317f1cd11f8ba12d3e1547a9f1
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Device Details

"Helin" direct fundus lens and accessories
TW: โ€œๆตท็ณโ€็›ดๆŽฅ็œผๅบ•้กๅŠ้™„ไปถ
Risk Class 2
Cancelled

Registration Details

2aa44d317f1cd11f8ba12d3e1547a9f1

DHA00602107406

Company Information

Product Details

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

M Ophthalmology

M.1570 Fundus Mirrors

import

Dates and Status

Jun 04, 2010

Jun 04, 2015

May 28, 2018

Cancellation Information

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