Reinforced Endotracheal Tube, Singel use - ARCSA Registration 13b799562917be4b00a7c73f90c4fdc5
Access comprehensive regulatory information for Reinforced Endotracheal Tube, Singel use in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID 13b799562917be4b00a7c73f90c4fdc5 and manufactured by FLEXICARE MEDICAL LTD.,. The device was registered on October 26, 2023.
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
II
13b799562917be4b00a7c73f90c4fdc5
Reinforced Endotracheal Tube, Singel use
ARCSA ID: 13b799562917be4b00a7c73f90c4fdc5
Device Classification
Risk Class
II
Product Type
Invasive
Brand Name
FLEXICARE
Commercial Name
TUBES, TRACHEALS
Registration Information
Analysis ID
13b799562917be4b00a7c73f90c4fdc5
Registration Date
October 26, 2023
Expiration Date
October 26, 2028
Product Use
SUPPLY OF OXYNENE AND/OR ANESTHETIC GASES
Manufacturer
City
MOUNTAIN ASH
Country
UNITED KINGDOM OF GREAT BRITAIN
Address
CYNON VALLEY BUSINESS PARK, MOUNTAIN ASH, CF45 4ER, UNITED KINGDOM
Product Owner
Name
FLEXICARE MEDICAL LIMITED
Country
UNITED KINGDOM OF GREAT BRITAIN
Authorized Representative