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LIQUIFORM UV PHOSPHORUS, HDL LE, BRAND: LABTEST - DIGEMID Registration DMDIV4501E

Access comprehensive regulatory information for LIQUIFORM UV PHOSPHORUS, HDL LE, BRAND: LABTEST in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV4501E and manufactured by LABTEST DIAGNOSTICA S/A. The device was registered on May 30, 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
DMDIV4501E
LIQUIFORM UV PHOSPHORUS, HDL LE, BRAND: LABTEST
DIGEMID ID: DMDIV4501E
Local name: Fร“SFORO UV LIQUIFORM, HDL LE, MARCA: LABTEST
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV4501E
Registration Date
May 30, 2022
Expiration Date
May 30, 2027
Creation Date
March 10, 2025
Manufacturer
Authorized Representative