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"Guise" modular part artificial hearing ossicles - Taiwan Registration 00bfbded7c8571fe799ce3660291827d

Access comprehensive regulatory information for "Guise" modular part artificial hearing ossicles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 00bfbded7c8571fe799ce3660291827d 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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00bfbded7c8571fe799ce3660291827d
Registration Details
Taiwan FDA Registration: 00bfbded7c8571fe799ce3660291827d
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Device Details

"Guise" modular part artificial hearing ossicles
TW: โ€œๅ‰ๆ–ฏโ€ๆจก็ต„ๅผ้ƒจๅˆ†ไบบๅทฅ่ฝๅฐ้ชจ
Risk Class 2
Cancelled

Registration Details

00bfbded7c8571fe799ce3660291827d

DHA00601805008

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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