Pure Global

"Stryker" intervertebral fusion device - Taiwan Registration aa8081e21bea3898d768fa20ea5cca11

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
1 Competitors
2 Recent Registrations
aa8081e21bea3898d768fa20ea5cca11
Registration Details
Taiwan FDA Registration: aa8081e21bea3898d768fa20ea5cca11
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Stryker" intervertebral fusion device
TW: โ€œๅฒ่ณฝๅ…‹โ€ๆคŽ้–“่žๅˆๅ™จ
Risk Class 2

Registration Details

aa8081e21bea3898d768fa20ea5cca11

DHA00601795602

Company Information

France

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

import

Dates and Status

Mar 23, 2007

Mar 23, 2027

Companies Making Similar Products
Top companies providing products similar to ""Stryker" intervertebral fusion device"