2019-NCOV ANTIGEN DETECTION KIT (FLUORESCENCE), 2019-NCOV ANTIGEN RAPID DETECTION KIT (LATERAL FLOW ASSAY). - DIGEMID Registration DMDIV4344E
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.
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DIGEMID Official Data
DMDIV4344E
2019-NCOV ANTIGEN DETECTION KIT (FLUORESCENCE), 2019-NCOV ANTIGEN RAPID DETECTION KIT (LATERAL FLOW ASSAY).
DIGEMID ID: DMDIV4344E
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
Authorized Representative

