Pure Global

FRESENIUS KABI S.A. - Authorized Company Profile

Explore comprehensive authorized company profile for FRESENIUS KABI S.A. through Pure Global AI's free Argentina medical device database. This company manufactures 119 medical devices registered with ANMAT across 8 registration types. Their registration history spans from Sep 01, 2017 to Jul 16, 2024.

This page provides detailed insights including recent registrations, registration type distribution (Class I-II Registration Modification: 37, Registration modification (non-agile) Class III-IV: 8, Revalidation of Registration I-II-III-IV: 26, 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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119 Devices
8 Registration Types
FRESENIUS KABI S.A.
Authorized Company
119
Total Devices
8
Registration Types
2017
Earliest
2024
Latest
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Recent Registrations
Latest 20 ANMAT device registrations

Continuous autotransfusion system

Sistema de autotransfusi贸n continuo

648-84

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

Feeding tube

Sonda de alimentaci贸n

648-80

Revalidation of Registration I-II-III-IV
May 30, 2024

Extension

Extensi贸n

648-89

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

Filters

Filtros

648-11

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

Transfusion set

Set de transfusi贸n

648-83

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

Infusion set

Set de infusi贸n

648-34

Class I-II Registration Modification
May 15, 2024

Ambulatory infusion pump

Bomba de infusi贸n ambulatoria

648-110

Registration Class III-IV
May 07, 2024

Filter

Filtro

648-111

Registration Class III-IV
Apr 22, 2024

Transfusion set

Set de transfusi贸n

648-83

Class I-II Registration Modification
Apr 11, 2024

Infusion set

Set de infusi贸n

648-35

Class I-II Registration Modification
Mar 15, 2024

Enteral pump delivery system for tube feeding

Sistema de administraci贸n para bomba enteral para alimentaci贸n por sonda

648-61

Class I-II Registration Modification
Mar 15, 2024

Anesthetic depth monitor and accessories.

Monitor de profundidad anest茅sica y accesorios.

648-79

Class I-II Registration Modification
Feb 21, 2024

Blood cell separator

Separador de c茅lulas sangu铆neas

648-105

Modification of Agile Registration Class III-IV
Feb 08, 2024

Enteral feeding syringe

Jeringa para alimentaci贸n enteral

648-82

Revalidation of Registration I-II-III-IV
Jan 29, 2024

Syringe Infusion Pumps

Bombas de Infusi贸n Mediante Jeringa

648-76

Revalidation of Registration I-II-III-IV
Jan 08, 2024

VL Infusion Set

Set de infusi贸n VL

648-27

Class I-II Registration Modification
Dec 19, 2023

Probe

Sonda

648-33

Revalidation of Registration I-II-III-IV
Dec 18, 2023

Parenteral nutrition bag

Bolsa de nutrici贸n parenteral

648-106

Class I-II Registration Modification
Dec 05, 2023

Connector

Conector

648-108

Class I-II Registration
Nov 29, 2023

Anesthetic depth monitor and accessories.

Monitor de profundidad anest茅sica y accesorios.

648-79

Revalidation of Registration I-II-III-IV
Nov 24, 2023
Registration Type Distribution
Devices by registration type
Class I-II Registration Modification
37
31.1% of total
Revalidation of Registration I-II-III-IV
26
21.8% of total
Class I-II Registration
20
16.8% of total
Modification of Agile Registration Class III-IV
11
9.2% of total
Registration modification (non-agile) Class III-IV
8
6.7% of total
Revalidation + Modification of Class I-II Registration
8
6.7% of total
Registration Class III-IV
7
5.9% of total
Class I-II Registration Revalidation
2
1.7% of total