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HBsAg TEST; HCV TEST; H.PYLORI Ab TEST; H.PYLORI Ag TEST; ROTAVIRUS Ag TEST CASSETTE; ROTAVIRUS AND ADENOVIRUS Ag TEST CASSETTE; MP IgM TEST; MULTI-DRUG 5 TEST PANEL; FECAL OCCULT BLOOD TEST, MARCA: CORETEST. - DIGEMID Registration DMDIV2617E

Access comprehensive regulatory information for HBsAg TEST; HCV TEST; H.PYLORI Ab TEST; H.PYLORI Ag TEST; ROTAVIRUS Ag TEST CASSETTE; ROTAVIRUS AND ADENOVIRUS Ag TEST CASSETTE; MP IgM TEST; MULTI-DRUG 5 TEST PANEL; FECAL OCCULT BLOOD TEST, MARCA: CORETEST. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV2617E and manufactured by CORE TECHNOLOGY CO., LTD.. The device was registered on March 16, 2018.

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
DMDIV2617E
HBsAg TEST; HCV TEST; H.PYLORI Ab TEST; H.PYLORI Ag TEST; ROTAVIRUS Ag TEST CASSETTE; ROTAVIRUS AND ADENOVIRUS Ag TEST CASSETTE; MP IgM TEST; MULTI-DRUG 5 TEST PANEL; FECAL OCCULT BLOOD TEST, MARCA: CORETEST.
DIGEMID ID: DMDIV2617E
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Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV2617E
Registration Date
March 16, 2018
Expiration Date
March 16, 2023
Creation Date
February 23, 2023
Authorized Representative