Pure Global

ampliCube STD Panel 3 - ARCSA Registration 2aa43cf3d203186dae6176eeae0023c9

Access comprehensive regulatory information for ampliCube STD Panel 3 in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 2aa43cf3d203186dae6176eeae0023c9 and manufactured by MIKROGEN GMBH. The device was registered on June 22, 2022.

This page provides complete registration details including product type (In Vitro Diagnostic), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.

Free Database
Powered by Pure Global AI
ARCSA Official Data
III
2aa43cf3d203186dae6176eeae0023c9
ampliCube STD Panel 3
ARCSA ID: 2aa43cf3d203186dae6176eeae0023c9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Risk Class
III
Product Type
In Vitro Diagnostic
Brand Name
MIKROGEN
Commercial Name
19-238 IVD Reagents/Kits, Molecular Assay, Infection, Bacteria
Registration Information
Analysis ID
2aa43cf3d203186dae6176eeae0023c9
Registration Date
June 22, 2022
Expiration Date
June 22, 2027
Product Use

THE AMPLICUBE STD PANEL 3 IS AN IN VITRO QUALITY TEST FOR THE SPECIFIC VERIFICATION OF THE DNA OF THE HERPES SIMPLEX VIRUS (TYPES 1/2) AND TREPONEMA PALLIDUM IN UROGENITAL SMEARS OF HUMAN ORIGIN.

Manufacturer
City
NEURIED
Country
GERMANY
Address
FLORIANSBOGEN 2-4, 82061 NEURIED, GERMANY
Product Owner
Name
MIKROGEN GMBH
Country
GERMANY
Authorized Representative
Address
AV. EUGENIO ESPEJO 2410 VIA A TANDA NAYON, PLAZA DEL RANCHO
Phone
987070898