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Authorized representative profile

Humiss International B.V.

EU EUDAMEDNetherlands740 represented devicesSRN NL-AR-000001490
VerifiedEUDAMED · official EU database
740
Total devices
3
Risk classes
2022
Earliest version
2025
Latest version
Regulatory footprint
Search Humiss International B.V. across other regulatory registries
ThailandColombiaSouth KoreaCanadaEcuadorSaudi Arabia
Recent products (latest 10)
Most recently updated devices in the database
Real-Time PCR System
06972168355015
Class A
Automatic Specific Proteins Analyzer
06972168353523
Class A
Automatic Chemiluminescence Analyzer
06972168351017
Class A
Semi-Automatic Urine Analyzer
06972168350188
Class A
Automatic Chemiluminescence Analyzer
06972168350140
Class A
Automatic Hematology Analyzer CC-5 Cell Clean A
06950617415367
Class A
Chemiluminescence Analyzer Reaction Cuvettes
06950617423454
Class A
Chemiluminescence Analyzer Wash Buffer
06950617423690
Class A
General Name: Coagulation Analyzer Sample Diluent（CASD)
06950617416821
Class A
Mag-Bind RNA Extraction Kit
06950617443452
Class A
Risk class distribution
Breakdown by risk classification
IVD General47964.7% of total
Class I22230.0% of total
Class A395.3% of total
Top manufacturers
Most common manufacturers represented by this AR
Maccura Biotechnology Co., Ltd.
65.1%482 devices
Ningbo KK-Bioscience Co., Ltd.
11.2%83 devices
Xiamen LongStar Medical Equipment Co., Ltd
8.0%59 devices
Junocare Medical Devices Ltd
6.6%49 devices
Tiangen Biotech (Beijing) Co., Ltd.
2.6%19 devices
About this profile

Explore comprehensive authorized representative profile for Humiss International B.V. through Pure Global AI's free EU medical device database. This organization represents 740 medical devices registered with EUDAMED across 3 risk classes based in Netherlands.

This page provides detailed insights including recent registrations, risk class distribution (Class I: 222, IVD General: 479, Class A: 39), 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.