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Antoni lumbar posterior fusion device - Taiwan Registration 2cbc3dc54bc5911e12c886b14f91dacc

Access comprehensive regulatory information for Antoni lumbar posterior 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 2cbc3dc54bc5911e12c886b14f91dacc and manufactured by SCIENT'X. The authorized representative in Taiwan is CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD..

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2cbc3dc54bc5911e12c886b14f91dacc
Registration Details
Taiwan FDA Registration: 2cbc3dc54bc5911e12c886b14f91dacc
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Device Details

Antoni lumbar posterior fusion device
TW: ไบžๆฑๅฐผ่…ฐๆคŽๅพŒ่ทฏ่žๅˆๅ™จ
Risk Class 2
Cancelled

Registration Details

2cbc3dc54bc5911e12c886b14f91dacc

DHA00601701208

Company Information

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

Aug 18, 2006

Aug 18, 2016

May 21, 2018

Cancellation Information

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