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SANGRILA 510S - ARCSA Registration b67e1b013dd8f99de5970b9a4ddcb306

Access comprehensive regulatory information for SANGRILA 510S in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID b67e1b013dd8f99de5970b9a4ddcb306 and manufactured by BEIJING AEONMED CO, LTD. The device was registered on January 07, 2021.

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
b67e1b013dd8f99de5970b9a4ddcb306
SANGRILA 510S
ARCSA ID: b67e1b013dd8f99de5970b9a4ddcb306
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Device Classification
Risk Class
III
Product Type
Active
Brand Name
.
Commercial Name
Ventilators
Registration Information
Analysis ID
b67e1b013dd8f99de5970b9a4ddcb306
Registration Date
January 07, 2021
Expiration Date
January 07, 2026
Product Use

THE VENTILATOR SYSTEM IS AIMED AT PROVIDING CONTINUOUS VENTILATION TREATMENT TO THE PATIENT AND MONITORING PATIENTS WITH RESPIRATORY FAILURE OR FAILURE AND REQUIRING RESPIRATORY SUPPORT.

Manufacturer
City
BEIJING
Country
CHINA
Address
ROOM 405, BASEMENT 1 TO 4TH FLOOR OF 901 UNIT, BUILDING 9, NO.26 OUTER RING WEST ROAD, FENGTAI DISTRICT, BEIJING 100070, CHINA
Product Owner
Name
BEIJING AEONMED CO, LTD
Country
CHINA
Authorized Representative
Address
AV ELOY ALFARO N32-656 AND RUSSIA TROYA BUILDING SECOND FLOOR
Phone
6007782