PRO 911 DEFIBRILLATOR, BRAND: AMELIFE - DIGEMID Registration DB8416E
Access comprehensive regulatory information for PRO 911 DEFIBRILLATOR, BRAND: AMELIFE in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DB8416E and manufactured by AMELIFE LLC. The device was registered on December 22, 2023.
This page provides complete registration details including product type (BIOMEDICAL EQUIPMENT), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.
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DIGEMID Official Data
DB8416E
PRO 911 DEFIBRILLATOR, BRAND: AMELIFE
DIGEMID ID: DB8416E
Local name: PRO 911 DEFIBRILLATOR, MARCA: AMELIFE
Device Classification
Product Type
BIOMEDICAL EQUIPMENT
Registration Information
Analysis ID
DB8416E
Registration Date
December 22, 2023
Expiration Date
December 22, 2028
Creation Date
March 10, 2025
Manufacturer
Name
AMELIFE LLCAuthorized Representative

