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"Jiayang" ureters - Taiwan Registration bd4a3c434241243fc069e8baf1850434

Access comprehensive regulatory information for "Jiayang" ureters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd4a3c434241243fc069e8baf1850434 and manufactured by URO TECHNOLOGY SDN BHD. The authorized representative in Taiwan is ANDERSON MEDICARE 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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bd4a3c434241243fc069e8baf1850434
Registration Details
Taiwan FDA Registration: bd4a3c434241243fc069e8baf1850434
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Device Details

"Jiayang" ureters
TW: โ€œไฝณๆด‹โ€ๅฐŽๅฐฟ็ฎก
Risk Class 2
Cancelled

Registration Details

bd4a3c434241243fc069e8baf1850434

DHA00602278607

Company Information

Malaysia

Product Details

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

H Gastroenterology and urology

H.5130 ๆณŒๅฐฟๅฐŽ็ฎกๅŠๅ…ถ้™„ไปถ

import

Dates and Status

Sep 09, 2011

Sep 09, 2021

Oct 12, 2023

Cancellation Information

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