TWINFIX ULTRA PK4.5MM W/2 UB-WHT &BL - ARCSA Registration 307482368cd9d6d0cdd59ffc207095a6
Access comprehensive regulatory information for TWINFIX ULTRA PK4.5MM W/2 UB-WHT &BL in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 307482368cd9d6d0cdd59ffc207095a6 and manufactured by SMITH & NEPHEW INC.. The device was registered on October 25, 2017.
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
IV
307482368cd9d6d0cdd59ffc207095a6
TWINFIX ULTRA PK4.5MM W/2 UB-WHT &BL
ARCSA ID: 307482368cd9d6d0cdd59ffc207095a6
Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
SMITH &NEPHEW
Commercial Name
Procedure Kits/Trays, Sutures
Registration Information
Analysis ID
307482368cd9d6d0cdd59ffc207095a6
Registration Date
October 25, 2017
Expiration Date
October 25, 2027
Product Use
SOFT TISSUE ATTACHMENT TO BONE
Manufacturer
Country
UNITED STATES
Address
150 MINUTEMAN ROAD ANDOVER, MASSACHUSETTS 01810, USA
Product Owner
Name
SMITH & NEPHEW INC ENDOSCOPY DIVISION
Country
UNITED STATES
Authorized Representative
Address
STREET: AVENIDA ORELLANA NUMBER: S/N INTERSECTION:AVENIDA AMAZONAS
Phone
2232060