Taiwan FDA registration aa8081e21bea3898d768fa20ea5cca11

"Stryker" intervertebral fusion device

TW: “史賽克”椎間融合器
Taiwan flagTaiwan·Risk Class 2·STRYKER SPINE SAS·Registered Mar 23, 2007 – Mar 23, 2027Active
Registration details
Analysis ID
aa8081e21bea3898d768fa20ea5cca11
Customs Code
DHA00601795602
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
Mar 23, 2007
Expiry Date
Mar 23, 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 aa8081e21bea3898d768fa20ea5cca11 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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