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"Jiahong" Noo intervertebral fusion device - Taiwan Registration fde36dbf618de48dd5f6c2ce84ce9576

Access comprehensive regulatory information for "Jiahong" Noo intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fde36dbf618de48dd5f6c2ce84ce9576 and manufactured by ALPHATEC SPINE INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

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fde36dbf618de48dd5f6c2ce84ce9576
Registration Details
Taiwan FDA Registration: fde36dbf618de48dd5f6c2ce84ce9576
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Device Details

"Jiahong" Noo intervertebral fusion device
TW: โ€œไฝณ้ดปโ€่ซพๆญๆคŽ้–“่žๅˆๅ™จ
Risk Class 2
Cancelled

Registration Details

fde36dbf618de48dd5f6c2ce84ce9576

DHA00602404402

Company Information

United States

Product Details

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

N Orthopedics

N.3060 ๆคŽ้ซ”้–“ไน‹่„ŠๆคŽ็Ÿฏๆญฃๅ›บๅฎš็‰ฉ

import

Dates and Status

Sep 25, 2012

Sep 25, 2022

Apr 12, 2024

Cancellation Information

Logged out

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