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"St. Yoda" inner catheter - Taiwan Registration 30b1975db66cbb34b3f5d652ae523bad

Access comprehensive regulatory information for "St. Yoda" inner catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30b1975db66cbb34b3f5d652ae523bad and manufactured by St. Jude Medical, Cardiac Rhythm Management Division. The authorized representative in Taiwan is Taiwan Shengyuda Medical Supplies 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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30b1975db66cbb34b3f5d652ae523bad
Registration Details
Taiwan FDA Registration: 30b1975db66cbb34b3f5d652ae523bad
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Device Details

"St. Yoda" inner catheter
TW: โ€œ่–็Œท้”โ€ๅ…งๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

30b1975db66cbb34b3f5d652ae523bad

DHA00601831202

Company Information

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 07, 2007

Sep 07, 2017

Nov 04, 2019

Cancellation Information

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