UNIFARMA S.A. - Authorized Company Profile

Explore comprehensive authorized company profile for UNIFARMA S.A. through Pure Global AI's free Argentina medical device database. This company manufactures 123 medical devices registered with ANMAT across 7 registration types. Their registration history spans from Jan 23, 2018 to Aug 13, 2024.

This page provides detailed insights including recent registrations, registration type distribution (Revalidation of Registration I-II-III-IV: 19, Class I-II Registration: 10, Registration modification (non-agile) Class III-IV: 35, 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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123 Devices

7 Registration Types

UNIFARMA S.A.

Authorized Company

123

Total Devices

7

Registration Types

2018

Earliest

2024

Latest

DJ Fang

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Recent Registrations

Latest 20 ANMAT device registrations

Sirolimus-Releasing Bioresorbable Vascular Scaffolding System

Sistema de armazón vascular biorreabsorbible liberador de Sirolimus

954-235

Registration Class III-IV

Vascular closure device

Dispositivo de cierre vascular

954-217

Registration Class III-IV

Locking system

Sistema de cierre

954-211

Registration Class III-IV

Sirolimus Coronary Elution Stent System

Sistema de stent coronario de elución de Sirolimus

954-168

Revalidation of Registration I-II-III-IV

Cobalt-chromium coronary stent system

Sistema de stent coronario de cromo-cobalto

954-127

Revalidation of Registration I-II-III-IV

Electroporation system

Sistema de electroporación

954-218

Modification of Agile Registration Class III-IV

Micro guide

Microguía

954-231

Registration Class III-IV

Transcatheter Heart Valve System

Sistema de válvula cardiaca transcateter

954-182

Registration modification (non-agile) Class III-IV

Neuro-thrombectomy system

Sistema de neuro-trombectomía

954-232

Registration Class III-IV

Coronary thrombectomy system

Sistema de trombectomia coronaria

954-233

Registration Class III-IV

Balloon Dilation Catheter for Percutaneous Transluminal Angioplasty

Catéter de dilatación con balón para Angioplastia Transluminal Percutánea

954-229

Class I-II Registration

Coronary Stent System

Sistema de endoprótesis coronario

954-109

Revalidation of Registration I-II-III-IV

Sirolimus Eluting Coronary Stent System

Sistema de stent coronario liberador de Sirolimus

954-129

Revalidation of Registration I-II-III-IV

Sirolimus-coated balloon catheter

Catéter con balón recubierto con Sirolimus

954-164

Revalidation of Registration I-II-III-IV

Left atrial appendage occluder

Oclusor de orejuela auricular izquierda

954-169

Revalidation of Registration I-II-III-IV

Hemodialysis equipment

Equipo para hemodiálisis

954-202

Registration Class III-IV

Hemostatic valve set

Set de válvula hemostática

954-224

Class I-II Registration Modification

Kit manifold

954-225

Class I-II Registration Modification

Self-expanding peripheral vascular stent

Stent vascular periférico autoexpandible

954-226

Registration Class III-IV

Trabectomy system

Sistema de trabectomia

954-179

Registration modification (non-agile) Class III-IV

Registration Type Distribution

Devices by registration type

Registration Class III-IV

41

33.3% of total

Registration modification (non-agile) Class III-IV

35

28.5% of total

Revalidation of Registration I-II-III-IV

19

15.4% of total

Class I-II Registration

10

8.1% of total

Class I-II Registration Modification

10

8.1% of total

Modification of Agile Registration Class III-IV

7

5.7% of total

Revalidation + Modification of Class I-II Registration

1

0.8% of total