Peru DIGEMID registration DMDIV4344E

2019-NCOV ANTIGEN DETECTION KIT (FLUORESCENCE), 2019-NCOV ANTIGEN RAPID DETECTION KIT (LATERAL FLOW ASSAY).

Name: 2019-NCOV ANTIGEN DETECTION KIT (FLUORESCENCE), 2019-NCOV ANTIGEN RAPID DETECTION KIT (LATERAL FLOW ASSAY). — DIGEMID registration DMDIV4344E
Creator: SUNBIO MEDICAL Co., Ltd.
Keywords: 2019-NCOV ANTIGEN DETECTION KIT (FLUORESCENCE), 2019-NCOV ANTIGEN RAPID DETECTION KIT (LATERAL FLOW ASSAY)., 2019-NCOV ANTIGEN DETECTION KIT (FLUORESCENCE), 2019-NCOV ANTIGEN RAPID DETECTION KIT (LATERAL FLOW ASSAY)., DMDIV4344E, IN VITRO MEDICAL DEVICE, SUNBIO MEDICAL Co., Ltd., DIGEMID registration

PeruIN VITRO MEDICAL DEVICESUNBIO MEDICAL Co., Ltd.Registered February 28, 2022

VerifiedDIGEMID · official registry

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV4344E
Registration Date: February 28, 2022
Expiration Date: February 28, 2027
Creation Date: March 10, 2025

Manufacturer

Name: SUNBIO MEDICAL Co., Ltd.

Authorized Representative

Name: DROGUERIA SAN DIEGO SOCIEDAD COMERCIAL DE RESPONSABILIDAD LIMITADA

About this record

Access comprehensive regulatory information for 2019-NCOV ANTIGEN DETECTION KIT (FLUORESCENCE), 2019-NCOV ANTIGEN RAPID DETECTION KIT (LATERAL FLOW ASSAY). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4344E and manufactured by SUNBIO MEDICAL Co., Ltd.. The device was registered on February 28, 2022.

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.