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"Imersian" developer injection system - Taiwan Registration 8390f4755675913640c1f4d1980f09ba

Access comprehensive regulatory information for "Imersian" developer injection system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8390f4755675913640c1f4d1980f09ba and manufactured by Bayer Medical Care Inc.;; IMAXEON PTY LTD.. The authorized representative in Taiwan is HSIEN TAI INSTRUMENTS 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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8390f4755675913640c1f4d1980f09ba
Registration Details
Taiwan FDA Registration: 8390f4755675913640c1f4d1980f09ba
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Device Details

"Imersian" developer injection system
TW: โ€œ็›Š้‚ๆฃฎโ€ ้กฏๅฝฑๅŠ‘ๆณจๅฐ„็ณป็ตฑ
Risk Class 2

Registration Details

8390f4755675913640c1f4d1980f09ba

DHA05603745801

Company Information

United States;;Australia

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1650 ่ก€็ฎกๆ”ๅฝฑๆณจๅฐ„ๅ™จๅ’Œๆณจๅฐ„็ญ’

Contract manufacturing;; input

Dates and Status

Nov 10, 2024

Nov 10, 2029