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"TPMT" Defibrillation Electrode (Non-Sterile) - Taiwan Registration ea6f82707e37a895584579d34a5edb43

Access comprehensive regulatory information for "TPMT" Defibrillation Electrode (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea6f82707e37a895584579d34a5edb43 and manufactured by ADVANCED MEDICAL DESIGN CO., LTD.. The authorized representative in Taiwan is TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC..

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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ea6f82707e37a895584579d34a5edb43
Registration Details
Taiwan FDA Registration: ea6f82707e37a895584579d34a5edb43
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Device Details

"TPMT" Defibrillation Electrode (Non-Sterile)
TW: "ๅฐ้†ซ" ๅŽป้กซ็”จ้›ปๆ“Š่ฒผ็‰‡
Risk Class 2
MD

Registration Details

ea6f82707e37a895584579d34a5edb43

Ministry of Health Medical Device Manufacturing No. 007427

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E5300 DC Defibrillator (with shock plate)

Produced in Taiwan, China; Contract manufacturing

Dates and Status

Mar 17, 2022

Mar 17, 2027