XPERT® XPRESS COV-2 PLUS. - DIGEMID Registration DMDIV4660E
Access comprehensive regulatory information for XPERT® XPRESS COV-2 PLUS. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4660E and manufactured by CEPHEID. The device was registered on September 26, 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
DMDIV4660E
XPERT® XPRESS COV-2 PLUS.
DIGEMID ID: DMDIV4660E
Local name: XPERT® XPRESS COV-2 PLUS.
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4660E
Registration Date
September 26, 2022
Expiration Date
September 26, 2027
Creation Date
March 10, 2025
Manufacturer
Name
CEPHEIDAuthorized Representative

