T-Cell Xtend® - ARCSA Registration f000a8d6abb1774791fc4ff19311f143
Access comprehensive regulatory information for T-Cell Xtend® in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID f000a8d6abb1774791fc4ff19311f143 and manufactured by OXFORD IMMUNOTEC LIMITED. The device was registered on June 09, 2023.
This page provides complete registration details including product type (In Vitro Diagnostic), 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
f000a8d6abb1774791fc4ff19311f143
T-Cell Xtend®
ARCSA ID: f000a8d6abb1774791fc4ff19311f143
Device Classification
Risk Class
III
Product Type
In Vitro Diagnostic
Commercial Name
19-041 IVD Reagents/Testing Kits, Serology, Bacteria
Registration Information
Analysis ID
f000a8d6abb1774791fc4ff19311f143
Registration Date
June 09, 2023
Expiration Date
June 09, 2028
Product Use
FOR USE IN THE PREPARATION AND ISOLATION OF PURIFIED LYMPHOCYTES DIRECTLY FROM WHOLE BLOOD.
Manufacturer
City
ABINGDON
Country
UNITED KINGDOM OF GREAT BRITAIN
Address
143 PARK DRIVE EAST, MILTON PARK, ABINGDON, OXFORDSHIRE, OX14 4SE, U.K
Product Owner
Name
OXFORD IMMUNOTEC LIMITED
Country
UNITED KINGDOM OF GREAT BRITAIN
Authorized Representative