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“Arthesys” Y-Connector - Taiwan Registration d496a5687c19205311581f3c9274b523

Access comprehensive regulatory information for “Arthesys” Y-Connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d496a5687c19205311581f3c9274b523 and manufactured by ARTHESYS. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..

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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d496a5687c19205311581f3c9274b523
Registration Details
Taiwan FDA Registration: d496a5687c19205311581f3c9274b523
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Device Details

“Arthesys” Y-Connector
TW: “亞提斯” Y型連接器
Risk Class 2
MD

Registration Details

d496a5687c19205311581f3c9274b523

Ministry of Health Medical Device Import No. 034464

DHA05603446407

Company Information

France

Product Details

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

E Cardiovascular devices

E4290 Arterial vascular bypass joint piston, multi-duct joint or accessory

Imported from abroad

Dates and Status

Mar 19, 2021

Mar 19, 2026