Taiwan FDA registration b9149128a79f7ebc93152e4dc75f7ab6

"Stryker" intervertebral fusion device

TW: “史賽克”椎間融合器
Taiwan flagTaiwan·Risk Class 2·STRYKER SPINE SAS·Registered Sep 20, 2007 – Sep 12, 2027Active
Registration details
Analysis ID
b9149128a79f7ebc93152e4dc75f7ab6
Customs Code
DHA00601832100
Company information
Manufacturer
STRYKER SPINE SAS
Manufacturer Country
France
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order.
Product Type (Level 1)
N Orthopedics
Import Information
import
Dates and status
Registration Date
Sep 20, 2007
Expiry Date
Sep 12, 2027
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About this record

Access comprehensive regulatory information for "Stryker" 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 b9149128a79f7ebc93152e4dc75f7ab6 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 SAS, and 2 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.

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