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"Stryker" clinical model - Taiwan Registration 5effdfff96cff120b0cf97c58a3a035c

Access comprehensive regulatory information for "Stryker" clinical model in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5effdfff96cff120b0cf97c58a3a035c and manufactured by STRYKER IRELAND LIMITED. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

This page provides complete technical specifications, regulatory compliance details. 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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5effdfff96cff120b0cf97c58a3a035c
Registration Details
Taiwan FDA Registration: 5effdfff96cff120b0cf97c58a3a035c
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Device Details

"Stryker" clinical model
TW: "ๅฒ่ณฝๅ…‹" ่‡จๅบŠ็”จๆจฃๆฟ
Risk Class 1
Cancelled

Registration Details

5effdfff96cff120b0cf97c58a3a035c

DHA04400245801

Company Information

Ireland

Product Details

Clinical templates consist of medical molds or probes that are used to select and configure implants for surgical plastic surgery or as guidelines before cutting tissue.

N Orthopedics

N.4800 Sample plate for clinical use

import

Dates and Status

Jan 04, 2006

Jan 04, 2011

Nov 06, 2012

Cancellation Information

Logged out

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