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L-OSTEOTOME - ARCSA Registration 915cde57171529bfd507e39bb33a3fea

Access comprehensive regulatory information for L-OSTEOTOME in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 915cde57171529bfd507e39bb33a3fea and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The device was registered on December 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
915cde57171529bfd507e39bb33a3fea
L-OSTEOTOME
ARCSA ID: 915cde57171529bfd507e39bb33a3fea
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Device Classification
Risk Class
I
Product Type
Invasive
Commercial Name
Instruments for Prosthesis Implantation, Orthopedic
Sterilization Method
NON-STERILE
Registration Information
Analysis ID
915cde57171529bfd507e39bb33a3fea
Registration Date
December 12, 2022
Expiration Date
December 12, 2027
Creation Date
December 14, 2022
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
TENNESSEE
Country
UNITED STATES
Address
1800 PYRAMID PLACE MEMPHIS TN, USA 38132
Product Owner
Name
MEDTRONIC INC
Country
UNITED STATES
Authorized Representative
Address
AV 23 RODRIGO CHAVEZ CIUDAD COLON
Phone
2232720