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"Stryker" femoral head - Taiwan Registration 92d7b12a5ee178f87be4a525960b6ec7

Access comprehensive regulatory information for "Stryker" femoral head in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92d7b12a5ee178f87be4a525960b6ec7 and manufactured by STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.. 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 HOWMEDICA OSTEONICS-STRYKER IRELAND, 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.

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92d7b12a5ee178f87be4a525960b6ec7
Registration Details
Taiwan FDA Registration: 92d7b12a5ee178f87be4a525960b6ec7
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Device Details

"Stryker" femoral head
TW: โ€œๅฒ่ณฝๅ…‹โ€่‚ก้ชจ้ ญ
Risk Class 2

Registration Details

92d7b12a5ee178f87be4a525960b6ec7

DHA05602970101

Company Information

Product Details

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

N Orthopedics

N.3350 Semi-restricted cormium/polymer-like cement-type supplements

Input;; Contract manufacturing

Dates and Status

Apr 26, 2017

Apr 26, 2027

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