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Medtronic Reusable Instruments - ARCSA Registration 26ef3fc8e73353e0522b8af10158f77e

Access comprehensive regulatory information for Medtronic Reusable Instruments in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 26ef3fc8e73353e0522b8af10158f77e and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The device was registered on September 28, 2023.

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
26ef3fc8e73353e0522b8af10158f77e
Medtronic Reusable Instruments
ARCSA ID: 26ef3fc8e73353e0522b8af10158f77e
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Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
Medtronic
Commercial Name
Instruments for Prosthesis Implantation, Orthopedic
Registration Information
Analysis ID
26ef3fc8e73353e0522b8af10158f77e
Registration Date
September 28, 2023
Expiration Date
September 28, 2028
Product Use

THE REUSABLE INSTRUMENTS ARE INTENDED FOR USE IN ORTHOPEDIC AND NEUROLOGICAL SURGICAL INTERVENTIONS TO MANIPULATE TISSUES AND BONE OR TO BE USED WITH OTHER DEVICES DURING SURGERY. IT IS POSSIBLE THAT SOME INSTRUMENT INCORPORATES A MEASUREMENT FUNCTION, WHOSE USES WILL BE DESCRIBED ON THE LABEL AND ON THE INSTRUMENT.

Manufacturer
City
TENESSE
Country
UNITED STATES
Address
1800 PYRAMID PLACE MEMPHIS, TN USA, 38132
Product Owner
Name
MEDTRONIC, INC
Country
UNITED STATES
Authorized Representative
Address
BLOCK: 274 STREET: AV. 23 RODRIGO CHAVEZ CONJUNTO: CIUDAD COLONNUMERO: S/N INTERSECCION:JUAN TANCA MARENGO
Phone
2232720