Pure Global

MOBILE C-ARM FOR IMAGE-GUIDED THERAPY - Argentina Medical Device Registration

Access comprehensive regulatory information for MOBILE C-ARM FOR IMAGE-GUIDED THERAPY in the Argentina medical device market through Pure Global AI's free database. This Revalidation of Registration I-II-III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on August 14, 2024.

This page provides complete registration details including product code (1103-263), brand name (PHILIPS), 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.

Free Database
Powered by Pure Global AI
Argentina ANMAT Data
Bilingual (Spanish/English)
Revalidation of Registration I-II-III-IV
MOBILE C-ARM FOR IMAGE-GUIDED THERAPY
ARCO EN C Mร“VIL PARA TERAPIA GUIADA POR IMรGENES
Argentina Medical Device Registration
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Manufacturers 1) y 2) Zenition 30 Zenition 50 Zenition 70 Zenition 90 Manufacturer 2) Zenition 10

Spanish:

De fabricantes 1) y 2) Zenition 30 Zenition 50 Zenition 70 Zenition 90 De fabricante 2) Zenition 10

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
1103-263
Brand Name
PHILIPS
Product Name
MOBILE C-ARM FOR IMAGE-GUIDED THERAPY
ARCO EN C Mร“VIL PARA TERAPIA GUIADA POR IMรGENES
Registration Information
Registration Date
August 14, 2024
Database ID
cmhayu5bd0kd8ekuz870qutto
Authorized Representative