Taiwan FDA registration 3caf4444f1b33448986264da0376c783

"Stryker" Aixveta intermediary catheter

TW: “史賽克” 艾克斯薇塔中介導管
Taiwan flagTaiwan·Risk Class 2·Stryker Neurovascular;; InNeuroCo·Registered Jul 25, 2023 – Jul 25, 2028Active
Registration details
Analysis ID
3caf4444f1b33448986264da0376c783
Customs Code
DHA05603657003
Company information
Manufacturer Country
United States
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1250 Percutaneous catheters
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Jul 25, 2023
Expiry Date
Jul 25, 2028
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About this record

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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