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"HERMANN" MANUAL SURGICAL INSTRUMENT FOR GENERAL USE(Non-Sterile) - Taiwan Registration 56c9990337df44970bd0f17f72fd60d2

Access comprehensive regulatory information for "HERMANN" MANUAL SURGICAL INSTRUMENT FOR GENERAL USE(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 56c9990337df44970bd0f17f72fd60d2 and manufactured by HANS HERMANN GMBH MEDIZINTEHNIK. The authorized representative in Taiwan is GUO YANG MEDICAL CO., LTD..

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56c9990337df44970bd0f17f72fd60d2
Registration Details
Taiwan FDA Registration: 56c9990337df44970bd0f17f72fd60d2
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Device Details

"HERMANN" MANUAL SURGICAL INSTRUMENT FOR GENERAL USE(Non-Sterile)
TW: "่ณ€่Œ" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

56c9990337df44970bd0f17f72fd60d2

Ministry of Health Medical Device Import No. 015120

DHA09401512001

Company Information

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Apr 16, 2015

Apr 16, 2020

Jun 22, 2022

Cancellation Information

Logged out

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