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"Sdio Tis" Titan guidewire - Taiwan Registration 362aa238de3b20cccc31b5a91752e8cd

Access comprehensive regulatory information for "Sdio Tis" Titan guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 362aa238de3b20cccc31b5a91752e8cd and manufactured by STEREOTAXIS, INC.. The authorized representative in Taiwan is UPWARDS BIOSYSTEMS 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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362aa238de3b20cccc31b5a91752e8cd
Registration Details
Taiwan FDA Registration: 362aa238de3b20cccc31b5a91752e8cd
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Device Details

"Sdio Tis" Titan guidewire
TW: โ€œๆ–ฏ่ฟชๅฅง้ˆฆๆ€โ€ๆณฐๅฆๅฐŽ็ตฒ
Risk Class 2
Cancelled

Registration Details

362aa238de3b20cccc31b5a91752e8cd

DHA00602132709

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1330 Catheter Guide Wires

import

Dates and Status

Aug 25, 2010

Aug 25, 2015

May 28, 2018

Cancellation Information

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