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ALLPLEX™ RV MASTER ASSAY, ALLPLEX™ CT/NG/MG/TV ASSAY, ALLPLEX™ GENITAL ULCER ASSAY, ALLPLEX™ GI PARASITE ASSAY, ALLPLEX™ CANDIDIASIS ASSAY, ALLPLEX™ RESPIRATORY PANEL 4, ANYPLEX™ II THROMBOSIS SNP PANEL ASSAY. - DIGEMID Registration DMDIV5112E

Access comprehensive regulatory information for ALLPLEX™ RV MASTER ASSAY, ALLPLEX™ CT/NG/MG/TV ASSAY, ALLPLEX™ GENITAL ULCER ASSAY, ALLPLEX™ GI PARASITE ASSAY, ALLPLEX™ CANDIDIASIS ASSAY, ALLPLEX™ RESPIRATORY PANEL 4, ANYPLEX™ II THROMBOSIS SNP PANEL ASSAY. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5112E and manufactured by SEEGENE INC.. The device was registered on September 06, 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.

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DIGEMID Official Data
DMDIV5112E
ALLPLEX™ RV MASTER ASSAY, ALLPLEX™ CT/NG/MG/TV ASSAY, ALLPLEX™ GENITAL ULCER ASSAY, ALLPLEX™ GI PARASITE ASSAY, ALLPLEX™ CANDIDIASIS ASSAY, ALLPLEX™ RESPIRATORY PANEL 4, ANYPLEX™ II THROMBOSIS SNP PANEL ASSAY.
DIGEMID ID: DMDIV5112E
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV5112E
Registration Date
September 06, 2023
Expiration Date
September 06, 2028
Creation Date
March 10, 2025
Manufacturer
Authorized Representative