"Stryker" cervical artificial disc - Taiwan Registration b5fb1726704eae58450dada5002fd451
Access comprehensive regulatory information for "Stryker" cervical artificial disc in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5fb1726704eae58450dada5002fd451 and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STRYKER SPINE SA, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
This product is indicated for the treatment of cervical radiculoradiculus symptoms (upper extremity pain and/or nerve damage) caused by loss of disc height, complications of disc/osteophytes, or single-level disc herniation between Neck 3 and Neck 7. This product is suitable for replacing a single-segment intervertebral disc between Neck 3 and Neck 7, increasing and maintaining the height of the intervertebral disc, relieving the terminal symptoms of the upper limbs, and improving the function of the treated vertebral segment to enable it to rotate.
N Orthopedics
import
Dates and Status
Mar 04, 2011
Mar 04, 2016
Apr 25, 2018
Cancellation Information
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