Pure Global

AMERICAN FIURE S.A. - Authorized Company Profile

Explore comprehensive authorized company profile for AMERICAN FIURE S.A. through Pure Global AI's free Argentina medical device database. This company manufactures 231 medical devices registered with ANMAT across 8 registration types. Their registration history spans from Sep 27, 2017 to Jul 17, 2024.

This page provides detailed insights including recent registrations, registration type distribution (Registration modification (non-agile) Class III-IV: 27, Class I-II Registration Modification: 77, Revalidation of Registration I-II-III-IV: 63, and more), and complete regulatory information from the official Argentina ANMAT (National Administration of Drugs, Foods and Medical Technology) medical device database with bilingual Spanish/English support. Pure Global AI offers free access to Argentina's complete medical device registry.

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231 Devices
8 Registration Types
AMERICAN FIURE S.A.
Authorized Company
231
Total Devices
8
Registration Types
2017
Earliest
2024
Latest
Pure Global
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Recent Registrations
Latest 20 ANMAT device registrations

Epidural needles

agujas epidurales

921-186

Revalidation of Registration I-II-III-IV
Jul 17, 2024

Needleless connectors for oncology drug administration

Conectores sin aguja para la administración de drogas oncológicas

921-232

Class I-II Registration Modification
Jun 13, 2024

TRACHEOTOMY KIT

KIT PARA TRAQUEOTOMIA

921-27

Revalidation of Registration I-II-III-IV
May 28, 2024

Cannulas for tracheotomy

Cánulas para traqueotomia

921-194

Revalidation of Registration I-II-III-IV
Apr 22, 2024

set of arterial catheterization

set de cateterismo arterial

921-197

Revalidation of Registration I-II-III-IV
Apr 18, 2024

tracheal tube

tubo traqueal

921-23

Revalidation of Registration I-II-III-IV
Apr 15, 2024

Epidural Filter

Filtro Epidural

921-47

Revalidation of Registration I-II-III-IV
Apr 15, 2024

intra-aortic balloon pump consoles (IABP)

consolas bombas balón intraaórtica (IABP)

921-85

Revalidation of Registration I-II-III-IV
Mar 27, 2024

Laryngeal mascara

Mascara laringea

921-41

Revalidation of Registration I-II-III-IV
Mar 25, 2024

Spinal needle

aguja espinal

921-51

Modification of Agile Registration Class III-IV
Mar 14, 2024

ARROWg+ard Blue Advance Midline

921-214

Modification of Agile Registration Class III-IV
Mar 14, 2024

Straight endobronchial tube

Tubo recto endobronquial

921-24

Revalidation of Registration I-II-III-IV
Jan 22, 2024

Bipolar balloon electrode catheter

catéter electrodo con balón bipolar

921-12

Revalidation of Registration I-II-III-IV
Jan 18, 2024

Flexible tip epidural catheter

cateter epidural de punta flexible

921-15

Revalidation of Registration I-II-III-IV
Jan 18, 2024

disinfection device

dispositivo de desinfeccion

921-196

Revalidation of Registration I-II-III-IV
Jan 16, 2024

Resistance loss device

dispositivo de perdida de resistencia

921-50

Revalidation of Registration I-II-III-IV
Jan 16, 2024

Cannulas for tracheotomy

Cánulas para traqueotomia

921-194

Class I-II Registration Modification
Dec 19, 2023

Phonation Valve

Válvula de Fonación

921-28

Revalidation of Registration I-II-III-IV
Dec 14, 2023

Spinal needle

aguja espinal

921-51

Revalidation of Registration I-II-III-IV
Dec 11, 2023

Lopez enteral valve

Valvula enteral Lopez

921-96

Revalidation of Registration I-II-III-IV
Dec 07, 2023
Registration Type Distribution
Devices by registration type
Class I-II Registration Modification
77
33.3% of total
Revalidation of Registration I-II-III-IV
63
27.3% of total
Registration modification (non-agile) Class III-IV
27
11.7% of total
Class I-II Registration
23
10.0% of total
Revalidation + Modification of Class I-II Registration
18
7.8% of total
Modification of Agile Registration Class III-IV
11
4.8% of total
Registration Class III-IV
9
3.9% of total
Class I-II Registration Revalidation
3
1.3% of total