Pure Global AI
Authorized representative profile

OSEN

EU EUDAMEDGermany12 represented devicesSRN DE-AR-000023626
VerifiedEUDAMED · official EU database
12
Total devices
1
Risk classes
2023
Earliest version
2023
Latest version
Regulatory footprint
Search OSEN across other regulatory registries
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Recent products (latest 10)
Most recently updated devices in the database
15 High-risk Human Papillomavirus DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)
06955792743526
IVD General
15 High-risk Human Papillomavirus DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)
06955792743533
IVD General
Monkeypox virus Nucleic Acid Diagnostic Kit (LAMP)
06955792743540
IVD General
Monkeypox virus Nucleic Acid Diagnostic Kit (LAMP)
06955792743557
IVD General
Monkeypox Virus (MPV) Rapid Antibody Test Kit (Immunochromatography Assay)
06955792743489
IVD General
Monkeypox Virus (MPV) Rapid Antibody Test Kit (Immunochromatography Assay)
06955792743496
IVD General
Monkeypox Virus (MPV) Rapid Antigen Test Kit (Immunochromatography Assay)
06955792743441
IVD General
Monkeypox Virus (MPV) Rapid Antibody Test Kit (Immunochromatography Assay)
06955792743519
IVD General
Monkeypox Virus (MPV) Rapid Antibody Test Kit (Immunochromatography Assay)
06955792743502
IVD General
Monkeypox Virus (MPV) Rapid Antigen Test Kit (Immunochromatography Assay)
06955792743458
IVD General
Risk class distribution
Breakdown by risk classification
IVD General12100.0% of total
Top manufacturers
Most common manufacturers represented by this AR
Sansure Biotech Inc.
100.0%12 devices
About this profile

Explore comprehensive authorized representative profile for OSEN through Pure Global AI's free EU medical device database. This organization represents 12 medical devices registered with EUDAMED across 1 risk class based in Germany.

This page provides detailed insights including recent registrations, risk class distribution (IVD General: 12), and complete regulatory information from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry.