URINE SEDIMENT ANALYZER REAGENT SHEATH, SHEATH, FUS SERIES URINALYSIS HYBRID SHEATH II, MARCA: DIRUI - DIGEMID Registration DMDIV4950E
Access comprehensive regulatory information for URINE SEDIMENT ANALYZER REAGENT SHEATH, SHEATH, FUS SERIES URINALYSIS HYBRID SHEATH II, MARCA: DIRUI in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4950E and manufactured by DIRUI INDUSTRIAL CO., LTD.. The device was registered on May 23, 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
DMDIV4950E
URINE SEDIMENT ANALYZER REAGENT SHEATH, SHEATH, FUS SERIES URINALYSIS HYBRID SHEATH II, MARCA: DIRUI
DIGEMID ID: DMDIV4950E
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4950E
Registration Date
May 23, 2023
Expiration Date
May 23, 2028
Creation Date
March 10, 2025
Manufacturer
Authorized Representative

