Pure Global

BIOSYSTEMS S.A. - Authorized Company Profile

Explore comprehensive authorized company profile for BIOSYSTEMS S.A. through Pure Global AI's free Argentina medical device database. This company manufactures 112 medical devices registered with ANMAT across 7 registration types. Their registration history spans from Nov 06, 2018 to Jun 12, 2024.

This page provides detailed insights including recent registrations, registration type distribution (Revalidation of Registration I-II-III-IV: 3, IVD Registration Group A and B: 79, Registration of products for IVD diagnostics - Group C and D: 19, 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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112 Devices
7 Registration Types
BIOSYSTEMS S.A.
Authorized Company
112
Total Devices
7
Registration Types
2018
Earliest
2024
Latest
Pure Global
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Recent Registrations
Latest 20 ANMAT device registrations

GeneProof Varicella-Zoster Virus (VZV) MC PCR Kit

626-215

Registration of products for IVD diagnostics - Group C and D
Jun 12, 2024

NGSgoยฎ-AmpX v2

626-210

Registration of products for IVD diagnostics - Group C and D
May 07, 2024

Allplexโ„ข Entero-DR Assay

626-213

Registration of products for IVD diagnostics - Group C and D
Apr 29, 2024

GeneProof Enterovirus PCR Kit

626-100

Agile modification of product registration for IVD diagnostics - Group C and D
Apr 08, 2024

GeneProof Adenovirus MC PCR Kit

626-214

IVD Registration Group A and B
Apr 04, 2024

NGSgo-MX6-1

626-190

Registration of products for IVD diagnostics - Group C and D
Jan 30, 2024

Allplexโ„ข HPV HR Detection

626-193

Registration of products for IVD diagnostics - Group C and D
Jan 30, 2024

NGSgoยฎ Library Full Kit

626-205

Registration of products for IVD diagnostics - Group C and D
Jan 29, 2024

HPV Direct Chip Kit

626-8492

Agile modification of product registration for IVD diagnostics - Group C and D
Jan 15, 2024

Allplexโ„ข CT/NG/MG/TV Assay

626-170

Non-agile modification of products for IVD diagnostics - Group C and D
Dec 20, 2023

Anyplexโ„ข HPV28 Detection

626-200

Agile modification of product registration for IVD diagnostics - Group C and D
Dec 11, 2023

Allplexโ„ข GI-EB Screening Assay

626-204

IVD Registration Group A and B
Dec 04, 2023

Anyplexโ„ข HPV28 Detection

626-200

Registration of products for IVD diagnostics - Group C and D
Nov 23, 2023

GeneProof Epstein-Barr Virus (EBV)MC PCR Kit

GeneProof Epstein-Barr Virus (EBV) MC PCR Kit

626-187

Registration of products for IVD diagnostics - Group C and D
Nov 06, 2023

NGSgo-MX11-3

626-191

Registration of products for IVD diagnostics - Group C and D
Oct 25, 2023

Allplex STI Essential Assay

626-166

Non-agile modification of products for IVD diagnostics - Group C and D
Sep 20, 2023

TANBead Nucleic Acid Extractor

626-206

IVD Registration Group A and B
Aug 25, 2023

Allplex โ„ข Vaginitis Screening Assay

626-167

Registration of products for IVD diagnostics - Group C and D
Aug 16, 2023

TANBead Nucleic Acid Extraction Kit (685 series)

626-201

IVD Registration Group A and B
Aug 16, 2023

Allplexโ„ข GI-Helminth(I) Assay

626-203

IVD Registration Group A and B
Aug 16, 2023
Registration Type Distribution
Devices by registration type
IVD Registration Group A and B
79
70.5% of total
Registration of products for IVD diagnostics - Group C and D
19
17.0% of total
Agile modification of product registration for IVD diagnostics - Group C and D
7
6.3% of total
Revalidation of Registration I-II-III-IV
3
2.7% of total
Non-agile modification of products for IVD diagnostics - Group C and D
2
1.8% of total
IVD Modification Group A and B
1
0.9% of total
Class I-II Registration Modification
1
0.9% of total