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MEDUCORE Standard con pulsoximetría en LIFE-BASE 1 NG XS - ARCSA Registration 7e0474a0f3cc0230e4ee57d98a6a75dc

Access comprehensive regulatory information for MEDUCORE Standard con pulsoximetría en LIFE-BASE 1 NG XS in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 7e0474a0f3cc0230e4ee57d98a6a75dc 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
7e0474a0f3cc0230e4ee57d98a6a75dc
MEDUCORE Standard con pulsoximetría en LIFE-BASE 1 NG XS
ARCSA ID: 7e0474a0f3cc0230e4ee57d98a6a75dc
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Device Classification
Risk Class
III
Product Type
Active
Brand Name
WEINMANN
Commercial Name
Defibrillators
Registration Information
Analysis ID
7e0474a0f3cc0230e4ee57d98a6a75dc
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