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"Baylis" Toronto atrial diaphragm catheter - Taiwan Registration 9c26e60d8d5eec1a1cd57fe94685f30d

Access comprehensive regulatory information for "Baylis" Toronto atrial diaphragm catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c26e60d8d5eec1a1cd57fe94685f30d and manufactured by BAYLIS MEDICAL COMPANY INC.. The authorized representative in Taiwan is CHINA SPRING TRADING 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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9c26e60d8d5eec1a1cd57fe94685f30d
Registration Details
Taiwan FDA Registration: 9c26e60d8d5eec1a1cd57fe94685f30d
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Device Details

"Baylis" Toronto atrial diaphragm catheter
TW: โ€œ่ฒๅˆฉๆ–ฏโ€ๅคšๅ€ซๅคšๆˆฟไธญ่†ˆๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

9c26e60d8d5eec1a1cd57fe94685f30d

DHA00601954501

Company Information

Canada

Product Details

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

E Cardiovascular Medicine Science

E.5175 Panectomy Conduit

import

Dates and Status

Dec 31, 2008

Dec 31, 2013

Aug 05, 2015

Cancellation Information

Logged out

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