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"Stryker" clinical sample (unsterilized) - Taiwan Registration 696845d023be21592265ca8af08151a1

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 696845d023be21592265ca8af08151a1 and manufactured by LISI MEDICAL ORTHOPAEDICS;; HOWMEDICA OSTEONICS CORP.. 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, ORTHOVITA INC.;; STRYKER LEIBINGER GMBH & CO. KG, 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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696845d023be21592265ca8af08151a1
Registration Details
Taiwan FDA Registration: 696845d023be21592265ca8af08151a1
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Device Details

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

Registration Details

696845d023be21592265ca8af08151a1

DHA09402320607

Company Information

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

QMS/QSD;; ๅง”่จ—่ฃฝ้€ ;; ่ผธๅ…ฅ

Dates and Status

Aug 07, 2023

Aug 07, 2028