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"Guise" all-titanium partially artificial hearing ossicle replacement - Taiwan Registration 5943295eaefb64fda0c5175ac723db96

Access comprehensive regulatory information for "Guise" all-titanium partially artificial hearing ossicle replacement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5943295eaefb64fda0c5175ac723db96 and manufactured by GYRUS ENT LLC, A WHOLLY OWNED SUBSIDIARY OF GYRUS ACMI, INC.. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.

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5943295eaefb64fda0c5175ac723db96
Registration Details
Taiwan FDA Registration: 5943295eaefb64fda0c5175ac723db96
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Device Details

"Guise" all-titanium partially artificial hearing ossicle replacement
TW: โ€œๅ‰ๆ–ฏโ€ๅ…จ้ˆฆ้ƒจๅˆ†ไบบๅทฅ่ฝๅฐ้ชจ็ฝฎๆ›็‰ฉ
Risk Class 2
Cancelled

Registration Details

5943295eaefb64fda0c5175ac723db96

DHA00601804808

Company Information

Product Details

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

G ENT Science

G.3450 Partial ossicular exchange

import

Dates and Status

May 01, 2007

May 01, 2017

Nov 20, 2019

Cancellation Information

Logged out

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