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"Stryker" Aixveta intermediary catheter - Taiwan Registration 3caf4444f1b33448986264da0376c783

Access comprehensive regulatory information for "Stryker" Aixveta intermediary catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3caf4444f1b33448986264da0376c783 and manufactured by Stryker Neurovascular;; InNeuroCo. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Stryker Neurovascular;; InNeuroCo, 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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3caf4444f1b33448986264da0376c783
Registration Details
Taiwan FDA Registration: 3caf4444f1b33448986264da0376c783
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Device Details

"Stryker" Aixveta intermediary catheter
TW: โ€œๅฒ่ณฝๅ…‹โ€ ่‰พๅ…‹ๆ–ฏ่–‡ๅก”ไธญไป‹ๅฐŽ็ฎก
Risk Class 2

Registration Details

3caf4444f1b33448986264da0376c783

DHA05603657003

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Contract manufacturing;; input

Dates and Status

Jul 25, 2023

Jul 25, 2028

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