Peru DIGEMID registration DMDIV4790E

COMBO DIAGNOSTIC RAPID TEST FOR SYPHILIS /HIV (1+2) (WHOLE BLOOD).

Name: COMBO DIAGNOSTIC RAPID TEST FOR SYPHILIS /HIV (1+2) (WHOLE BLOOD). — DIGEMID registration DMDIV4790E
Creator: NANTONG EGENS BIOTECHNOLOGY CO., LTD.
Keywords: COMBO DIAGNOSTIC RAPID TEST FOR SYPHILIS /HIV (1+2) (WHOLE BLOOD)., COMBO DIAGNOSTIC RAPID TEST FOR SYPHILIS /HIV (1+2) (WHOLE BLOOD)., DMDIV4790E, IN VITRO MEDICAL DEVICE, NANTONG EGENS BIOTECHNOLOGY CO., LTD., DIGEMID registration

PeruIN VITRO MEDICAL DEVICENANTONG EGENS BIOTECHNOLOGY CO., LTD.Registered January 10, 2023

VerifiedDIGEMID · official registry

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV4790E
Registration Date: January 10, 2023
Expiration Date: January 10, 2028
Creation Date: March 10, 2025

Manufacturer

Name: NANTONG EGENS BIOTECHNOLOGY CO., LTD.

Authorized Representative

Name: LS MEDISUR PERU S.A.C.

About this record

Access comprehensive regulatory information for COMBO DIAGNOSTIC RAPID TEST FOR SYPHILIS /HIV (1+2) (WHOLE BLOOD). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4790E and manufactured by NANTONG EGENS BIOTECHNOLOGY CO., LTD.. The device was registered on January 10, 2023.

This page provides complete registration details including product type (IN VITRO MEDICAL DEVICE), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.