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"Stryker" lumbar artificial disc - Taiwan Registration a687a6f76bc5c7a7be26ce4ddd311497

Access comprehensive regulatory information for "Stryker" lumbar artificial disc in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a687a6f76bc5c7a7be26ce4ddd311497 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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a687a6f76bc5c7a7be26ce4ddd311497
Registration Details
Taiwan FDA Registration: a687a6f76bc5c7a7be26ce4ddd311497
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Device Details

"Stryker" lumbar artificial disc
TW: โ€œๅฒ่ณฝๅ…‹โ€่…ฐๆคŽไบบๅทฅๆคŽ้–“็›ค
Risk Class 3
Cancelled

Registration Details

a687a6f76bc5c7a7be26ce4ddd311497

DHA00601944102

Company Information

France

Product Details

Indicated for the treatment of lumbar discogenic pain associated with degenerative disc disease (DDD). Replacing a single lumbar disc (L1-S1) with degenerative disease allows flexibility in the portion to be treated, improves function, and reduces back pain associated with DDD.

N Orthopedics

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

import

Dates and Status

Sep 17, 2008

Sep 17, 2013

Nov 15, 2016

Cancellation Information

Logged out

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