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MEDIUM UNIVERSAL CATHETER CLAMPING DEVICE - ARCSA Registration 1152d780fc81bc0f13f0d2b0dc835a9d

Access comprehensive regulatory information for MEDIUM UNIVERSAL CATHETER CLAMPING DEVICE in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 1152d780fc81bc0f13f0d2b0dc835a9d 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
1152d780fc81bc0f13f0d2b0dc835a9d
MEDIUM UNIVERSAL CATHETER CLAMPING DEVICE
ARCSA ID: 1152d780fc81bc0f13f0d2b0dc835a9d
Local name: DISPOSITIVO DE SUJECIÓN DE CATÉTER UNIVERSAL MEDIANO
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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
1152d780fc81bc0f13f0d2b0dc835a9d
Registration Date
November 23, 2022
Expiration Date
November 23, 2027
Creation Date
November 23, 2022
Product Use

IT IS A DISPOSABLE STABILIZATION DEVICE THAT SECURELY FIXES CATHETERS, TUBES AND LINES AT THE SITE.

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