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KARL STORZ AIDA - ARCSA Registration 7ea97c9e0bc4273217ee173134cfaff1

Access comprehensive regulatory information for KARL STORZ AIDA in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 7ea97c9e0bc4273217ee173134cfaff1 and manufactured by KARL STORZ SE & CO. KG. The device was registered on May 25, 2022.

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
I
7ea97c9e0bc4273217ee173134cfaff1
KARL STORZ AIDA
ARCSA ID: 7ea97c9e0bc4273217ee173134cfaff1
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Device Classification
Risk Class
I
Product Type
Active
Brand Name
AIDA® / AIDA™ mini / OR1™ . AVM / AIDA® C / SMARTSCREEN®
Commercial Name
Image Information, Archiving and Communication Systems
Registration Information
Analysis ID
7ea97c9e0bc4273217ee173134cfaff1
Registration Date
May 25, 2022
Expiration Date
May 25, 2027
Creation Date
May 25, 2022
Product Use

DOCUMENTATION SYSTEM (HARDWARE AND SOFTWARE) FOR AUDIOVISUAL DATA AND PATIENT DATA DURING DIAGNOSIS OR THERAPEUTIC INTERVENTION (RECEPTION AND SENDING OF AUDIO AND VIDEO SIGNALS)

Manufacturer
City
TUTTLINGEN
Country
GERMANY
Address
DR.-KARL-STORZ-STRASSE 34, 78532 TUTTLINGEN
Product Owner
Name
KARL STORZ SE & CO. KG
Country
GERMANY
Authorized Representative
Address
THE ISLAND N31-12 AND SAN GABRIEL
Phone
23936000