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"Stryker" ultrasound surgical device - Taiwan Registration 3597475e295bd3db891b8adb7b22bb8a

Access comprehensive regulatory information for "Stryker" ultrasound surgical device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3597475e295bd3db891b8adb7b22bb8a and manufactured by STRYKER LEIBINGER GMBH & CO. KG;; Stryker Instruments. 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 INSTRUMENTS;; STRYKER MEDTECH K.K., 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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3597475e295bd3db891b8adb7b22bb8a
Registration Details
Taiwan FDA Registration: 3597475e295bd3db891b8adb7b22bb8a
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Device Details

"Stryker" ultrasound surgical device
TW: โ€œๅฒ่ณฝๅ…‹โ€่ถ…้Ÿณๆณขๆ‰‹่ก“่ฃ็ฝฎ
Risk Class 2

Registration Details

3597475e295bd3db891b8adb7b22bb8a

DHA05602738405

Company Information

Product Details

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

I General, Plastic Surgery and Dermatology

I.0003 Ultrasound surgical device

import

Dates and Status

May 12, 2015

May 12, 2030

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