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"Medtronic" median bone plate fixation system - Taiwan Registration e81283c368a4300c622be08c5c8912cd

Access comprehensive regulatory information for "Medtronic" median bone plate fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e81283c368a4300c622be08c5c8912cd and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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e81283c368a4300c622be08c5c8912cd
Registration Details
Taiwan FDA Registration: e81283c368a4300c622be08c5c8912cd
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Device Details

"Medtronic" median bone plate fixation system
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๆญฃไธญ็ฝฎ็‰ฉ้ชจๆฟๅ›บๅฎš็ณป็ตฑ
Risk Class 2

Registration Details

e81283c368a4300c622be08c5c8912cd

DHA00601997105

Company Information

United States

Product Details

The Medtronic median placement laminoplasty system is used in laminoplasty of the lower cervical and upper thoracic spine (C3 to T3) to support bone grafts used to perform laminoplasty to prevent the graft material from being squeezed out or invaded to spinal nerves.

N Orthopedics

import

Dates and Status

Mar 24, 2009

Mar 24, 2029