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CENTRAL VENOUS CATHETER - ARCSA Registration fb7dd168cdf9b3d30cae7d4702263deb

Access comprehensive regulatory information for CENTRAL VENOUS CATHETER in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID fb7dd168cdf9b3d30cae7d4702263deb and manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.. The device was registered on September 25, 2019.

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
III
fb7dd168cdf9b3d30cae7d4702263deb
CENTRAL VENOUS CATHETER
ARCSA ID: fb7dd168cdf9b3d30cae7d4702263deb
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Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
ABLE
Commercial Name
CATHETERS, VASCULAR, FOR HEMODIALYSIS, IN CENTRAL VEINS
Sterilization Method
EO ETHYLENE OXIDE GAS
Registration Information
Analysis ID
fb7dd168cdf9b3d30cae7d4702263deb
Registration Date
September 25, 2019
Expiration Date
September 25, 2024
Creation Date
December 15, 2021
Product Use

THEY ARE INTENDED FOR INFUSION OF VASCULAR ACCESS AND EXTRACTION OF BLOOD, BLOOD PRODUCTS AND LIQUIDS, PLASMA APHERESIS.

Manufacturer
City
FOSHAN
Country
CHINA
Address
NO. 89 , TAOYUAN EAST ROAD, NANHAI , FOSHAN , GUANGDONG PROVINCE, CHINA
Product Owner
Name
GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.
Country
CHINA
Authorized Representative
Address
CDLA. TORRES DEL SALADO, MZ 46 SOLAR 3
Phone
42442306