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"Heini" direct fundus lens and accessories - Taiwan Registration ee42a5a45a3f2a0d08c2924abe09f995

Access comprehensive regulatory information for "Heini" 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 ee42a5a45a3f2a0d08c2924abe09f995 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is Poussen Industrial Limited.

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ee42a5a45a3f2a0d08c2924abe09f995
Registration Details
Taiwan FDA Registration: ee42a5a45a3f2a0d08c2924abe09f995
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Device Details

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

Registration Details

ee42a5a45a3f2a0d08c2924abe09f995

DHA00601811803

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 12, 2007

Jun 12, 2012

May 05, 2014

Cancellation Information

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