Taiwan FDA registration 064feefb7723863ea7f00d7227f15b28

"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 Jun 24, 2024 – Jun 24, 2029Active
Registration details
Analysis ID
064feefb7723863ea7f00d7227f15b28
Customs Code
DHA05603731301
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
Input;; Contract manufacturing
Dates and status
Registration Date
Jun 24, 2024
Expiry Date
Jun 24, 2029
Companies making similar products

Top companies providing products similar to ""Stryker" Aixveta intermediary catheter"

Recent registrations

Recently registered similar products

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 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations