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"Stryker" Aixveta intermediary catheter - Taiwan Registration 064feefb7723863ea7f00d7227f15b28

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 064feefb7723863ea7f00d7227f15b28 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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064feefb7723863ea7f00d7227f15b28
Registration Details
Taiwan FDA Registration: 064feefb7723863ea7f00d7227f15b28
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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

064feefb7723863ea7f00d7227f15b28

DHA05603731301

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Input;; Contract manufacturing

Dates and Status

Jun 24, 2024

Jun 24, 2029

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