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Rapid test for the qualitative detection of antibodies against Treponema pallidum - Argentina Medical Device Registration

Access comprehensive regulatory information for Rapid test for the qualitative detection of antibodies against Treponema pallidum in the Argentina medical device market through Pure Global AI's free database. This Registration of products for IVD diagnostics - Group C and D medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on July 20, 2023.

This page provides complete registration details including product code (1102-224), brand name (Wiener lab.), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.

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Registration of products for IVD diagnostics - Group C and D
Rapid test for the qualitative detection of antibodies against Treponema pallidum
Prueba r谩pida para la detecci贸n cualitativa de anticuerpos contra Treponema pallidum
Argentina Medical Device Registration
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Device Classification
Registration Type
Registration of products for IVD diagnostics - Group C and D
Registro De Productos Para Diagn贸stico IVD - Grupo C Y D
Product Code
1102-224
Brand Name
Wiener lab.
Product Name
Rapid test for the qualitative detection of antibodies against Treponema pallidum
Prueba r谩pida para la detecci贸n cualitativa de anticuerpos contra Treponema pallidum
Registration Information
Registration Date
July 20, 2023
Database ID
cmhayu4fw0jr4ekuz3xr5lk9l
Documents
Authorized Representative
Name
WIENER Laboratories S.A.I.C.
WIENER Laboratorios S.A.I.C.