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"Stryker" clinical sample (unsterilized) - Taiwan Registration 64c6b781a381e913f6ef94c937beff2d

Access comprehensive regulatory information for "Stryker" clinical sample (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 64c6b781a381e913f6ef94c937beff2d and manufactured by K2M, INC.. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including STRYKER GMBH, LISI MEDICAL ORTHOPAEDICS;; HOWMEDICA OSTEONICS CORP., and 4 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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64c6b781a381e913f6ef94c937beff2d
Registration Details
Taiwan FDA Registration: 64c6b781a381e913f6ef94c937beff2d
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Device Details

"Stryker" clinical sample (unsterilized)
TW: "ๅฒ่ณฝๅ…‹" ่‡จๅบŠ็”จๆจฃๆฟ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

64c6b781a381e913f6ef94c937beff2d

DHA09402326803

Company Information

United States

Product Details

Limited to the classification and grading management measures of medical equipment "Clinical Use Model (N.4800) First Level Identification Range".

N Orthopedics

N.4800 Sample plate for clinical use

Input;; QMS/QSD

Dates and Status

Oct 05, 2023

Oct 05, 2028