CODMAN® - ARCSA Registration e325c6b54a70fb7a444e5657c0e9fced
Access comprehensive regulatory information for CODMAN® in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID e325c6b54a70fb7a444e5657c0e9fced and manufactured by INTEGRA LIFESCIENCES PRODUCTION CORPORATION. The device was registered on March 24, 2015.
This page provides complete registration details including product type (Invasive), 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
IV
e325c6b54a70fb7a444e5657c0e9fced
CODMAN®
ARCSA ID: e325c6b54a70fb7a444e5657c0e9fced
Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
CODMAN
Commercial Name
Derivations, for Hydrocephalus, Totals.
Registration Information
Analysis ID
e325c6b54a70fb7a444e5657c0e9fced
Registration Date
March 24, 2015
Expiration Date
March 24, 2025
Product Use
IN SYSTEMS DESIGNED TO DERIVE BY SHUNT, CEREBROSPINAL FLUID (CSF)
Manufacturer
City
MASSACHUSETTS
Country
UNITED STATES
Address
11 CABOT BLVD. MANSFIELD, MA USA 02048
Product Owner
Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Country
UNITED STATES
Authorized Representative