“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.
Device Details
Registration Details
9fcda88e2b5272656498eb874ec3378b
Ministry of Health Medical Device Import No. 025222
DHA05602522208
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

