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ORTHOSCAN MOBILE DI (MDI) MINI C-ARM - ARCSA Registration f56fb0f902203dc75bcff5e8245a532e

Access comprehensive regulatory information for ORTHOSCAN MOBILE DI (MDI) MINI C-ARM in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID f56fb0f902203dc75bcff5e8245a532e and manufactured by ZHIEHM-ORTHOSCAN, INC. The device was registered on November 14, 2023.

This page provides complete registration details including product type (Active), 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
f56fb0f902203dc75bcff5e8245a532e
ORTHOSCAN MOBILE DI (MDI) MINI C-ARM
ARCSA ID: f56fb0f902203dc75bcff5e8245a532e
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Device Classification
Risk Class
III
Product Type
Active
Brand Name
ORTHOSCAN
Commercial Name
IMAGE INTENSIFIERS
Registration Information
Analysis ID
f56fb0f902203dc75bcff5e8245a532e
Registration Date
November 14, 2023
Expiration Date
November 14, 2028
Product Use

THE ORTHOSCAN MOBILE DI MINI C-ARM FLUOROSCOPIC X-RAY IMAGING SYSTEM IS DESIGNED TO PROVIDE THE CLINICIAN WITH GENERAL FLUOROSCOPIC VISUALIZATION OF THE PATIENT, INCLUDING, BUT NOT LIMITED TO, SURGERY, ORTHOPEDIC PROCEDURES, AND CRITICAL AND EMERGENCY CARE PROCEDURES. THE MOBILE DI IS DESIGNED FOR USE IN ADULTS AND ADOLESCENTS TO DETECT AND DIAGNOSE FRACTURES AND OTHER TYPES OF LIMB IRREGULARITIES.

Manufacturer
City
ARIZONA
Country
UNITED STATES
Address
14555 N 82ND STREETSCOTTSDALE, ARIZONA 85260 UNITED STATES
Product Owner
Name
ZHIEHM-ORTHOSCAN, INC
Country
UNITED STATES
Authorized Representative
Address
AV 6 DE DICIEMBRE N24 417 AND LUIS CORDERO
Phone
992799222