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Chromsystems Instruments & Chemicals GmbH

US

Last updated May 23, 2026

What Chromsystems Instruments & Chemicals GmbH makes

Chromsystems Instruments & Chemicals GmbH produces in vitro diagnostic (IVD) reagents, kits, calibrators, and controls for liquid chromatography analysis, including high-performance chromatography columns. Their portfolio covers biogenic amine neurotransmitter testing (e.g., HVA, VMA, 5HIAA) and therapeutic drug monitoring controls for anticonvulsants and multi-therapy regimens. Microplate-based IVD solutions and urine/plasma/serum controls are also part of their offerings.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are intended for use in clinical laboratories and diagnostic settings, adhering to relevant regulatory standards for IVD performance and safety.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Chromsystems Instruments & Chemicals GmbH manufacture?

Chromsystems Instruments & Chemicals GmbH specializes in in vitro diagnostic (IVD) devices primarily used for liquid chromatography analysis. Their portfolio includes high-performance liquid chromatography analyser columns, reagents, kits, calibrators, and controls for biogenic amine neurotransmitter testing (such as HVA, VMA, and 5HIAA) as well as therapeutic drug monitoring controls for anticonvulsants and multi-therapy regimens. They also produce microplate-based IVD solutions and controls for urine, plasma, and serum samples, all designed for clinical laboratory and diagnostic use.

Where is Chromsystems Instruments & Chemicals GmbH based?

Chromsystems Instruments & Chemicals GmbH is based in the United States. While the company’s headquarters or primary operational location isn’t specified, their devices are regulated under U.S. FDA guidelines, indicating their market focus and compliance framework.

Which regulatory registries list Chromsystems Instruments & Chemicals GmbH’s devices?

Chromsystems Instruments & Chemicals GmbH’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for their Class I and Class II IVD products, which are intended for clinical and diagnostic applications. The UDI system helps track and verify device details for regulatory and quality purposes.

How are Chromsystems Instruments & Chemicals GmbH’s devices classified under FDA regulations?

Chromsystems Instruments & Chemicals GmbH’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body system it interacts with, as outlined in FDA’s regulatory framework for IVDs.

AI-generated from registry data and not verified by a human reviewer.

Information

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US
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Catalogue (590)

Page 3 of 12
DeviceModel / ReferenceRegistriesClassStatus
Plasma Calibration Standard 68003
FDA UDI
Class IIActive
Saliva Control 0349
FDA UDI
Class IUnknown
Urine Control 0139
FDA UDI
Class IActive
Plasma Control Bi-Level 0261
FDA UDI
Class IActive
Urine Control 0368
FDA UDI
Class IActive
Urine Calibrator Set 80839
FDA UDI
Class IIActive
Serum Control 0160
FDA UDI
Class IActive
Precolumn Cartridge 18051
FDA UDI
Class IActive
Plasma Calibration Standard 27034
FDA UDI
Class IIActive
Plasma Control Bi-Level 0147
FDA UDI
Class IActive
Reagent 81007
FDA UDI
Class IActive
Dried Blood Control 0197
FDA UDI
Class IActive
Reagent 81002
FDA UDI
Class IActive
Serum Control Bi-Level 0065
FDA UDI
Class IActive
Accessorie 80058
FDA UDI
Class IActive
Plasma Control Bi-Level 0094
FDA UDI
Class IActive
Reagent 6006/A9
FDA UDI
Class IActive
Reagent 5005
FDA UDI
Class IActive
Trap Column 62110/Epi
FDA UDI
Class IActive
Accessorie 5007
FDA UDI
Class IActive
Accessorie 2028/A
FDA UDI
Class IActive
Reagent 80810
FDA UDI
Class IActive
Whole Blood Control 0034
FDA UDI
Class IActive
Plasma Calibration Standard 5009
FDA UDI
Class IIActive
Precolumn Cartridge 18041
FDA UDI
Class IActive
Reagent Kit 34034/Premix
FDA UDI
Class IActive
Plasma Calibrator Set 81039
FDA UDI
Class IIActive
Plasma Control Bi-Level 0237
FDA UDI
Class IActive
Reagent Kit 6000/A5
FDA UDI
Class IActive
Precolumn Cartridge 17049
FDA UDI
Class IActive
Urine Calibrator Set 80639
FDA UDI
Class IIActive
HPLC Column 26100
FDA UDI
Class IActive
Plasma Control 0042
FDA UDI
Class IActive
Plasma Control Bi-Level 0227/XT2
FDA UDI
Class IActive
Serum Control 0338
FDA UDI
Class IActive
Precolumn Cartridge 18066
FDA UDI
Class IActive
Plasma Control 0247
FDA UDI
Class IActive
Plasma Control 0225
FDA UDI
Class IActive
Plasma Control 0228/XT2
FDA UDI
Class IActive
Urine Control 0372
FDA UDI
Class IActive
Analytical Column 80200
FDA UDI
Class IActive
HPLC Column 44100
FDA UDI
Class IActive
Serum Calibration Standard 22005/HR
FDA UDI
Class IIActive
Plasma Calibration Standard 49031
FDA UDI
Class IIActive
Analytical Column 62120
FDA UDI
Class IActive
HPLC Column 2130/COMBI
FDA UDI
Class IActive
HPLC Column 66100
FDA UDI
Class IActive
Reagent 3035
FDA UDI
Class IActive
HPLC Column 25100
FDA UDI
Class IActive
Plasma Control 0333
FDA UDI
Class IActive

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Chromsystems Instruments & Chemicals Gmbh Gräfelfing Bavaria · DE FEI 3003951180