Peru DIGEMID registration DMDIV4243E
D - DIMER RAPID QUANTITATIVE TEST (IMMUNOFLUORESCENCE ASSAY); HBA1C (GLYCATED HEMOGLOBIN) RAPID QUANTITATIVE TEST (IMMUNOFLUORESCENCE ASSAY).
Device classification
- Product Type
- IN VITRO MEDICAL DEVICE
Registration information
- Analysis ID
- DMDIV4243E
- Registration Date
- December 28, 2021
- Expiration Date
- December 28, 2026
- Creation Date
- March 10, 2025
Manufacturer
- Name
- AEHEALTH LIMITED
Authorized Representative
About this record
Access comprehensive regulatory information for D - DIMER RAPID QUANTITATIVE TEST (IMMUNOFLUORESCENCE ASSAY); HBA1C (GLYCATED HEMOGLOBIN) RAPID QUANTITATIVE TEST (IMMUNOFLUORESCENCE ASSAY). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4243E and manufactured by AEHEALTH LIMITED. The device was registered on December 28, 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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