OR3O DUAL MOBILITY TRIAL INSERT 22/36 - ARCSA Registration 7f58362a79a023f7f624d53d8a25b5be
Access comprehensive regulatory information for OR3O DUAL MOBILITY TRIAL INSERT 22/36 in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 7f58362a79a023f7f624d53d8a25b5be and manufactured by SMITH & NEPHEW, INC.. The device was registered on October 12, 2022.
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
I
7f58362a79a023f7f624d53d8a25b5be
OR3O DUAL MOBILITY TRIAL INSERT 22/36
ARCSA ID: 7f58362a79a023f7f624d53d8a25b5be
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
OR3O
Commercial Name
Instruments for Prosthesis Implantation
Registration Information
Analysis ID
7f58362a79a023f7f624d53d8a25b5be
Registration Date
October 12, 2022
Expiration Date
October 12, 2027
Product Use
FOR TOTAL HIP REPLACEMENT
Manufacturer
Product Owner
Name
SMITH & NEPHEW, INC.
Country
UNITED STATES
Authorized Representative
Address
STREET: AVENIDA ORELLANA NUMBER: S/N INTERSECTION:AVENIDA AMAZONAS
Phone
2232060