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"Stryker" intervertebral fusion device - Taiwan Registration b9149128a79f7ebc93152e4dc75f7ab6

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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b9149128a79f7ebc93152e4dc75f7ab6
Registration Details
Taiwan FDA Registration: b9149128a79f7ebc93152e4dc75f7ab6
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Device Details

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

Registration Details

b9149128a79f7ebc93152e4dc75f7ab6

DHA00601832100

Company Information

France

Product Details

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

N Orthopedics

import

Dates and Status

Sep 20, 2007

Sep 12, 2027

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