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MEDUCORE Standard with pulse oximetry on LIFE-BASE 4 NG - ARCSA Registration 696a56810df60b209770b935fa5da3a7

Access comprehensive regulatory information for MEDUCORE Standard with pulse oximetry on LIFE-BASE 4 NG in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 696a56810df60b209770b935fa5da3a7 and manufactured by WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG. The device was registered on May 31, 2018.

This page provides complete registration details including product type (Active), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.

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ARCSA Official Data
III
696a56810df60b209770b935fa5da3a7
MEDUCORE Standard with pulse oximetry on LIFE-BASE 4 NG
ARCSA ID: 696a56810df60b209770b935fa5da3a7
Local name: MEDUCORE Standard con pulsoximetría sobre LIFE-BASE 4 NG
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Device Classification
Risk Class
III
Product Type
Active
Brand Name
WEINMANN
Commercial Name
Defibrillators
Registration Information
Analysis ID
696a56810df60b209770b935fa5da3a7
Registration Date
May 31, 2018
Expiration Date
May 31, 2028
Product Use

DEFIBRILLATION/MONITORING SYSTEM FOR SEMIAUTOMATIC DEFIBRILLATION

Manufacturer
City
HAMBURG
Country
GERMANY
Address
FROHBOSESTRABE 12 22525
Product Owner
Name
WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG
Country
GERMANY
Authorized Representative
Address
CALL: OFF. LOS SHYRIS NUMERO: SN INTERSECCION:OFF. PORTUGAL
Phone
23825185