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"Guise" modular fully artificial hearing ossicle replacement - Taiwan Registration 25349183c3649a363ec355540e99ed91

Access comprehensive regulatory information for "Guise" modular fully 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 25349183c3649a363ec355540e99ed91 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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25349183c3649a363ec355540e99ed91
Registration Details
Taiwan FDA Registration: 25349183c3649a363ec355540e99ed91
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Device Details

"Guise" modular fully artificial hearing ossicle replacement
TW: โ€œๅ‰ๆ–ฏโ€ ๆจก็ต„ๅผๅ…จไบบๅทฅ่ฝๅฐ้ชจ็ฝฎๆ›็‰ฉ
Risk Class 2
Cancelled

Registration Details

25349183c3649a363ec355540e99ed91

DHA00601810701

Company Information

Product Details

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

G ENT Science

G.3495 Whole-hearing ossicle exchange

import

Dates and Status

Jun 01, 2007

Jun 01, 2017

Nov 20, 2019

Cancellation Information

Logged out

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