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“Skintact” Multifunction Defibrillation Electrode - Taiwan Registration 9fcda88e2b5272656498eb874ec3378b

Access comprehensive regulatory information for “Skintact” Multifunction Defibrillation Electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9fcda88e2b5272656498eb874ec3378b and manufactured by LEONHARD LANG GMBH. The authorized representative in Taiwan is SOPHYHZM MEDICAL INSTRUMENT 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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Registration Details
Taiwan FDA Registration: 9fcda88e2b5272656498eb874ec3378b
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Device Details

“Skintact” Multifunction Defibrillation Electrode
TW: “施肯貼克”去顫器用電擊貼片
Risk Class 2
MD
Cancelled

Registration Details

9fcda88e2b5272656498eb874ec3378b

Ministry of Health Medical Device Import No. 025222

DHA05602522208

Company Information

Austria

Product Details

E Cardiovascular devices

E5300 DC Defibrillator (with shock plate)

Imported from abroad

Dates and Status

Aug 07, 2013

Aug 07, 2018

Jun 07, 2022

Cancellation Information

Logged out

許可證已逾有效期