Peru DIGEMID registration DMDIV0931E

DIRECT GLYCOHEMOGLOBIN (HBA1C); GLYCOHEMOGLOBIN (PRE-FIL®); HEMA-SCREEN.

Peru·IN VITRO MEDICAL DEVICE·STANBIO LABORATORY·Registered June 15, 2009

Device classification

Product Type: IN VITRO MEDICAL DEVICE

Registration information

Analysis ID: DMDIV0931E
Registration Date: June 15, 2009
Expiration Date: June 15, 2029
Creation Date: March 10, 2025

Manufacturer

Name: STANBIO LABORATORY

Authorized Representative

Name: W.P. BIOMED SOCIEDAD ANONIMA

About this record

Access comprehensive regulatory information for DIRECT GLYCOHEMOGLOBIN (HBA1C); GLYCOHEMOGLOBIN (PRE-FIL®); HEMA-SCREEN. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV0931E and manufactured by STANBIO LABORATORY. The device was registered on June 15, 2009.

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.