Contrast Medium Injection Manifold Kits - ARCSA Registration 501974200a50bd69df7b22c245ed63da
Access comprehensive regulatory information for Contrast Medium Injection Manifold Kits in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 501974200a50bd69df7b22c245ed63da and manufactured by LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD. The device was registered on November 08, 2022.
This page provides complete registration details including product type (No 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
501974200a50bd69df7b22c245ed63da
Contrast Medium Injection Manifold Kits
ARCSA ID: 501974200a50bd69df7b22c245ed63da
Device Classification
Risk Class
I
Product Type
No Invasive
Brand Name
Rayband™, Angiopower™, Angioway™, Angiospring™
Commercial Name
MULTIPLE TUBES, FOR LIQUIDS
Sterilization Method
ETHYLENE OXIDE
Registration Information
Analysis ID
501974200a50bd69df7b22c245ed63da
Registration Date
November 08, 2022
Expiration Date
November 08, 2027
Creation Date
August 11, 2022
Product Use
ACCESSORY SYSTEM USED IN SURGICAL OPERATIONS
Manufacturer
City
BEIJING
Country
CHINA
Address
NO.37 CHAOQIAN ROAD, CHANGPING DISTRICT, BEIJING, 102200, P.R. CHINA
Product Owner
Name
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD
Country
CHINA
Authorized Representative