ANYPLEX™ II MTB/MDR DETECTION, ANYPLEX™ II MTB/XDR DETECTION. - DIGEMID Registration DMDIV5425E
Access comprehensive regulatory information for ANYPLEX™ II MTB/MDR DETECTION, ANYPLEX™ II MTB/XDR DETECTION. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV5425E and manufactured by SEEGENE INC.. The device was registered on March 25, 2024.
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
DMDIV5425E
ANYPLEX™ II MTB/MDR DETECTION, ANYPLEX™ II MTB/XDR DETECTION.
DIGEMID ID: DMDIV5425E
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV5425E
Registration Date
March 25, 2024
Expiration Date
March 25, 2029
Creation Date
March 10, 2025
Manufacturer
Name
SEEGENE INC.Authorized Representative

