XPERT® XPRESS COV-2 PLUS, MARCA: CEPHEID® - DIGEMID Registration DMDIV4709E
Access comprehensive regulatory information for XPERT® XPRESS COV-2 PLUS, MARCA: CEPHEID® in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4709E and manufactured by CEPHEID. The device was registered on October 21, 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
DMDIV4709E
XPERT® XPRESS COV-2 PLUS, MARCA: CEPHEID®
DIGEMID ID: DMDIV4709E
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4709E
Registration Date
October 21, 2022
Expiration Date
October 21, 2027
Creation Date
February 17, 2025
Manufacturer
Name
CEPHEIDAuthorized Representative

