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FOLEY CATHETER SECURING DEVICE - ARCSA Registration f7554bc2a44f64a1840f9ed92b176ad7

Access comprehensive regulatory information for FOLEY CATHETER SECURING DEVICE in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID f7554bc2a44f64a1840f9ed92b176ad7 and manufactured by TIDI PRODUCTS, LLC. The device was registered on November 23, 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
f7554bc2a44f64a1840f9ed92b176ad7
FOLEY CATHETER SECURING DEVICE
ARCSA ID: f7554bc2a44f64a1840f9ed92b176ad7
Local name: DISPOSITIVO DE ASGURAMIENTO DE CATÉTER FOLEY
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Device Classification
Risk Class
I
Product Type
No Invasive
Brand Name
GRIP LOK
Commercial Name
FASTENERS
Sterilization Method
GAMMA RADIATION
Registration Information
Analysis ID
f7554bc2a44f64a1840f9ed92b176ad7
Registration Date
November 23, 2022
Expiration Date
November 23, 2027
Creation Date
November 23, 2022
Product Use

IT IS A DISPOSABLE STABILIZATION DEVICE THAT FIXES THE CONNECTORS OF THE CATHETER AND PICC CONCENTRATORS FIRMLY IN PLACE

Manufacturer
City
NEENAH
Country
UNITED STATES
Address
570 ENTERPRISE DRIVE, NEENAH, WI 54956
Product Owner
Name
TIDI PRODUCTS, LLC
Country
UNITED STATES
Authorized Representative
Address
MURGEON STREET OE1-106 AND JORGE JUAN
Phone
22345627