NEW ASKIR 230 12V BR - ARCSA Registration 77ebf67526aa7169f65d7a3e4d7a757f
Access comprehensive regulatory information for NEW ASKIR 230 12V BR in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID 77ebf67526aa7169f65d7a3e4d7a757f and manufactured by CA-MI S.R.L.. The device was registered on December 09, 2020.
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
II
77ebf67526aa7169f65d7a3e4d7a757f
NEW ASKIR 230 12V BR
ARCSA ID: 77ebf67526aa7169f65d7a3e4d7a757f
Device Classification
Risk Class
II
Product Type
Active
Brand Name
CA-MI
Commercial Name
Aspirators, Surgical
Sterilization Method
NON-STERILE
Registration Information
Analysis ID
77ebf67526aa7169f65d7a3e4d7a757f
Registration Date
December 09, 2020
Expiration Date
December 09, 2025
Creation Date
November 24, 2022
Product Use
SURGICAL ASPIRATOR
Manufacturer
Product Owner
Name
CA-MI S.R.L.
Country
ITALY
Authorized Representative