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"Stryker" Cardille Remote Guided Catheter - Taiwan Registration 9e2ea8b02b4f79f0e710905839c33b2f

Access comprehensive regulatory information for "Stryker" Cardille Remote Guided Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e2ea8b02b4f79f0e710905839c33b2f and manufactured by Stryker Neurovascular. 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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9e2ea8b02b4f79f0e710905839c33b2f
Registration Details
Taiwan FDA Registration: 9e2ea8b02b4f79f0e710905839c33b2f
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Device Details

"Stryker" Cardille Remote Guided Catheter
TW: โ€œๅฒ่ณฝๅ…‹โ€ๅกๅพ—ๆจ‚้ ็ซฏๅผ•ๅฐŽๅฐŽ็ฎก
Risk Class 2

Registration Details

9e2ea8b02b4f79f0e710905839c33b2f

DHA05602999100

Company Information

Ireland;;United States

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Jul 31, 2017

Jul 31, 2027