FOLEY CATHETER SECURING DEVICE
- Risk class
- I
- Product type
- No Invasive
- Brand name
- GRIP LOK
- Commercial name
- FASTENERS
- Sterilization method
- GAMMA RADIATION
- Analysis ID
- f7554bc2a44f64a1840f9ed92b176ad7
- Registration date
- November 23, 2022
- Expiration date
- November 23, 2027
- Creation date
- November 23, 2022
- City
- NEENAH
- Country
- UNITED STATES
- Address
- 570 ENTERPRISE DRIVE, NEENAH, WI 54956
- Name
- TIDI PRODUCTS, LLC
- Country
- UNITED STATES
- Address
- MURGEON STREET OE1-106 AND JORGE JUAN
- Phone
- 22345627
IT IS A DISPOSABLE STABILIZATION DEVICE THAT FIXES THE CONNECTORS OF THE CATHETER AND PICC CONCENTRATORS FIRMLY IN PLACE
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.