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“Baylis” NRG Transseptal Needle - Taiwan Registration 2071bd339796013bdb7543c3f697c733

Access comprehensive regulatory information for “Baylis” NRG Transseptal Needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2071bd339796013bdb7543c3f697c733 and manufactured by BAYLIS MEDICAL COMPANY INC.. The authorized representative in Taiwan is WIN CHAMP MEDICAL 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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2071bd339796013bdb7543c3f697c733
Registration Details
Taiwan FDA Registration: 2071bd339796013bdb7543c3f697c733
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Device Details

“Baylis” NRG Transseptal Needle
TW: “貝利斯”心房中膈穿刺針
Risk Class 2
MD

Registration Details

2071bd339796013bdb7543c3f697c733

Ministry of Health Medical Device Import No. 032894

DHA05603289409

Company Information

Canada

Product Details

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

E Cardiovascular devices

E5175 Middle diaphragmectom catheter

Imported from abroad

Dates and Status

Oct 07, 2019

Oct 07, 2024