SS 12/14 TPR FEM HD 32MM -3 - ARCSA Registration c46c11d58dd271a02c4dfeb02b2dcda7
Access comprehensive regulatory information for SS 12/14 TPR FEM HD 32MM -3 in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID c46c11d58dd271a02c4dfeb02b2dcda7 and manufactured by SMITH & NEPHEW ORTHOPAEDICS GMBH. The device was registered on January 31, 2020.
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
III
c46c11d58dd271a02c4dfeb02b2dcda7
SS 12/14 TPR FEM HD 32MM -3
ARCSA ID: c46c11d58dd271a02c4dfeb02b2dcda7
Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
FEMORAL HEADS
Commercial Name
Test Prosthesis, Joint
Registration Information
Analysis ID
c46c11d58dd271a02c4dfeb02b2dcda7
Registration Date
January 31, 2020
Expiration Date
January 31, 2025
Product Use
TOTAL HIP ARTHROPLASTY SYSTEM
Manufacturer
Product Owner
Name
SMTIH & NEPHEW, INC.
Country
UNITED STATES
Authorized Representative
Address
STREET: AVENIDA ORELLANA NUMBER: S/N INTERSECTION:AVENIDA AMAZONAS
Phone
2232060