OCTAX LASERSHOT M, OCTAX NAVILASE and OCTAX NAVILASE UPGRADE, BRAND: VITROLIFE - DIGEMID Registration DB8873E
Access comprehensive regulatory information for OCTAX LASERSHOT M, OCTAX NAVILASE and OCTAX NAVILASE UPGRADE, BRAND: VITROLIFE in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DB8873E and manufactured by VITROLIFE GMBH. The device was registered on July 22, 2024.
This page provides complete registration details including product type (BIOMEDICAL EQUIPMENT), 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
DB8873E
OCTAX LASERSHOT M, OCTAX NAVILASE and OCTAX NAVILASE UPGRADE, BRAND: VITROLIFE
DIGEMID ID: DB8873E
Local name: OCTAX LASERSHOT M, OCTAX NAVILASE y OCTAX NAVILASE UPGRADE, MARCA: VITROLIFE
Device Classification
Product Type
BIOMEDICAL EQUIPMENT
Registration Information
Analysis ID
DB8873E
Registration Date
July 22, 2024
Expiration Date
July 22, 2029
Creation Date
February 10, 2025
Manufacturer
Name
VITROLIFE GMBHAuthorized Representative

