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Infusion pump AME-900 - ARCSA Registration 2327c15e33b9b58bea6245909094786f

Access comprehensive regulatory information for Infusion pump AME-900 in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 2327c15e33b9b58bea6245909094786f and manufactured by AMELIFE LLC.. The device was registered on May 18, 2022.

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
2327c15e33b9b58bea6245909094786f
Infusion pump AME-900
ARCSA ID: 2327c15e33b9b58bea6245909094786f
Local name: Bomba de infusión AME-900
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Device Classification
Risk Class
III
Product Type
Active
Brand Name
AMELIFE
Commercial Name
Infusion Pumps, Multitherapy
Sterilization Method
NOT APPLICABLE
Registration Information
Analysis ID
2327c15e33b9b58bea6245909094786f
Registration Date
May 18, 2022
Expiration Date
May 18, 2027
Creation Date
May 18, 2022
Product Use

THE INFUSION PUMP IS USED TOGETHER WITH THE INFUSION SET TO CONTROL THE DOSE OF LIQUID THAT PENETRATES THE PATIENT'S BODY, FOR EXAMPLE, INTRAVENOUS INFUSION.

Manufacturer
City
DELAWARE
Country
UNITED STATES
Address
8 THE GRN STE 7302 DOVER, DELAWARE, ESTADOS UNIDOS DE AMERICA
Product Owner
Name
AMELIFE LLC.
Country
UNITED STATES
Authorized Representative
Address
CIUDADELA CIUDAD DEL RIO SOLAR 8-1 CALLE NUMA POMPILIOLLONA S/N INTERSECCION RIO GUAYAS
Phone
44632290