SARS-COV-2 NEUTRALIZING ANTIBODIES TEST KIT (DRY FLUORESCENCE IMMUNOASSAY), MARCA: LANSIONBIO - DIGEMID Registration DMDIV4117E
Access comprehensive regulatory information for SARS-COV-2 NEUTRALIZING ANTIBODIES TEST KIT (DRY FLUORESCENCE IMMUNOASSAY), MARCA: LANSIONBIO in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4117E and manufactured by LANSION BIOTECHNOLOGY Co., Ltd.. The device was registered on October 01, 2021.
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
DMDIV4117E
SARS-COV-2 NEUTRALIZING ANTIBODIES TEST KIT (DRY FLUORESCENCE IMMUNOASSAY), MARCA: LANSIONBIO
DIGEMID ID: DMDIV4117E
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4117E
Registration Date
October 01, 2021
Expiration Date
October 01, 2026
Creation Date
February 10, 2025
Manufacturer
Authorized Representative

