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"Yatrien" Cleaved exchange therapy with perfusion catheter - Taiwan Registration 5bc73283bca4a131c20ac9e90f07c98a

Access comprehensive regulatory information for "Yatrien" Cleaved exchange therapy with perfusion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5bc73283bca4a131c20ac9e90f07c98a and manufactured by ATRIUM MEDICAL CORPORATION. The authorized representative in Taiwan is Hong Kong Synmei Co., Ltd. Taiwan Branch.

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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5bc73283bca4a131c20ac9e90f07c98a
Registration Details
Taiwan FDA Registration: 5bc73283bca4a131c20ac9e90f07c98a
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Device Details

"Yatrien" Cleaved exchange therapy with perfusion catheter
TW: โ€œไบž็ฟ ๆฉโ€ๅ…‹้‡Œ่ก›ไบคๆ›ๆฒป็™‚็”จ็ŒๆณจๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

5bc73283bca4a131c20ac9e90f07c98a

DHA00601923400

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Sep 25, 2008

Sep 25, 2013

Aug 13, 2015

Cancellation Information

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