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"Sdio Tis" Pegesas guidewire - Taiwan Registration be5bed06bceff3756694be89c0415069

Access comprehensive regulatory information for "Sdio Tis" Pegesas guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be5bed06bceff3756694be89c0415069 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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be5bed06bceff3756694be89c0415069
Registration Details
Taiwan FDA Registration: be5bed06bceff3756694be89c0415069
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Device Details

"Sdio Tis" Pegesas guidewire
TW: โ€œๆ–ฏ่ฟชๅฅง้ˆฆๆ€โ€ไฝฉๆ ผ่–ฉๆ–ฏๅฐŽ็ตฒ
Risk Class 2
Cancelled

Registration Details

be5bed06bceff3756694be89c0415069

DHA00602144107

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

Sep 07, 2010

Sep 07, 2020

Aug 05, 2022

Cancellation Information

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