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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

Country
US
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Catalogue (590)

Page 2 of 12
DeviceModel / ReferenceRegistriesClassStatus
Serum Calibration Standard 28006
FDA UDI
Class IIActive
Reagent 80605
FDA UDI
Class IActive
Accessorie 2028
FDA UDI
Class IActive
HPLC Column 37110
FDA UDI
Class IActive
Reagent 1011
FDA UDI
Class IActive
Whole Blood Control 0167
FDA UDI
Class IActive
Plasma Control 0133
FDA UDI
Class IActive
Reagent 4007
FDA UDI
Class IActive
Serum Calibration Standard 22005
FDA UDI
Class IIActive
Reagent Kit 34900/F
FDA UDI
Class IActive
Accessorie 34757
FDA UDI
Class IActive
Urine Control 0145
FDA UDI
Class IActive
HPLC Column 68100
FDA UDI
Class IActive
Reagent 6004/A5
FDA UDI
Class IActive
Reagent 1077/A5
FDA UDI
Class IActive
Plasma Control 0184
FDA UDI
Class IActive
Reagent Kit 44000
FDA UDI
Class IActive
Reagent 34006
FDA UDI
Class IActive
Reagent 3031
FDA UDI
Class IActive
Reagent 2033
FDA UDI
Class IActive
Calibration Standard 5003
FDA UDI
Class IIActive
Analytical Column 69100
FDA UDI
Class IActive
Whole Blood Control 0078
FDA UDI
Class IActive
Plasma Calibrator Set 92026/XT
FDA UDI
Class IIUnknown
HPLC Column 41100
FDA UDI
Class IActive
Urine Control 0369
FDA UDI
Class IActive
HPLC Column 38910
FDA UDI
Class IActive
Saliva Calibrator Set 73039
FDA UDI
Class IIUnknown
HPLC Column 5130
FDA UDI
Class IActive
Basic Kit 6000-C-BK
FDA UDI
Class IActive
Analytical Column 93100
FDA UDI
Class IActive
Accessorie 1008
FDA UDI
Class IActive
Plasma Control Bi-Level 0054
FDA UDI
Class IUnknown
Reagent Kit 1000/B/A9
FDA UDI
Class IActive
Dried Blood Control 0196
FDA UDI
Class IActive
Plasma Calibration Standard 28007
FDA UDI
Class IIActive
Reagent 80604/5
FDA UDI
Class IActive
Basic Kit 34400-BK
FDA UDI
Class IActive
Serum Control 0340
FDA UDI
Class IActive
Reagent 80604
FDA UDI
Class IActive
Reagent 1005/A5
FDA UDI
Class IActive
Reagent Kit 80800
FDA UDI
Class IActive
Reagent 44004
FDA UDI
Class IActive
Urine Calibrator Set 80739
FDA UDI
Class IIActive
Serum Calibration Standard 32003
FDA UDI
Class IIActive
Plasma Calibrator Set 92052
FDA UDI
Class IIActive
Reagent Kit 81000
FDA UDI
Class IActive
Urine Calibration Standard 41003
FDA UDI
Class IIActive
Precolumn Cartridge 15012
FDA UDI
Class IActive
Urine Control Bi-Level 0316
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