Peru DIGEMID registration DMDIV4501E

LIQUIFORM UV PHOSPHORUS, HDL LE, BRAND: LABTEST

Local name: FÓSFORO UV LIQUIFORM, HDL LE, MARCA: LABTEST

Peru·IN VITRO MEDICAL DEVICE·LABTEST DIAGNOSTICA S/A·Registered May 30, 2022

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

Name: LABTEST DIAGNOSTICA S/A

Authorized Representative

Name: SIGMALAB S.A.C.

About this record

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.