13 Types of High-Risk Human Papillomavirus Nucleic Acid Detection Kit (PCR-fluorescence Probing) - ARCSA Registration dabac7239bf6a368fe1820d4d917c0d2
Access comprehensive regulatory information for 13 Types of High-Risk Human Papillomavirus Nucleic Acid Detection Kit (PCR-fluorescence Probing) in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID dabac7239bf6a368fe1820d4d917c0d2 and manufactured by TRIPLEX INTERNATIONAL BIOSCIENCES (CHINA) CO., LTD.. The device was registered on January 12, 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.
KIT FOR THE QUALITATIVE IN VITRO DETECTION OF 13 SUBTYPES OF HUMAN PAPILLOMAVIRUS (HPV) (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59 AND 68) IN EXFOLIATED CELLS FROM WART CELL SAMPLES AND URETHRAL SECRETION.