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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 6 of 12
DeviceModel / ReferenceRegistriesClassStatus
Precolumn Cartridge 18035
FDA UDI
Class IActive
Calibration Standard 3033
FDA UDI
Class IIActive
Urine Control 0376
FDA UDI
Class IActive
Accessorie 34760
FDA UDI
Class IActive
Reagent 80002
FDA UDI
Class IActive
Whole Blood Control 0024
FDA UDI
Class IActive
Urine Control 0318
FDA UDI
Class IActive
Analytical Column 72110
FDA UDI
Class IActive
Reagent Kit 1000/B/A1
FDA UDI
Class IActive
Saliva Control 0350
FDA UDI
Class IUnknown
Plasma Control 0073
FDA UDI
Class IActive
Plasma Control Bi-Level 0264
FDA UDI
Class IActive
Reagent 2024
FDA UDI
Class IActive
Reagent 2027
FDA UDI
Class IActive
Precolumn Cartridge 18047
FDA UDI
Class IActive
Reagent Kit 6000-C
FDA UDI
Class IActive
Plasma Control 0010
FDA UDI
Class IActive
Whole Blood Calibration Standard 52003
FDA UDI
Class IIActive
Urine Hydrolysis Control Set 0470
FDA UDI
Class IActive
Plasma Calibrator Set 46039/XL
FDA UDI
Class IIActive
Plasma Control 0236
FDA UDI
Class IActive
Reagent 32006
FDA UDI
Class IActive
Plasma Control Bi-Level 0057
FDA UDI
Class IUnknown
Urine Control 0474
FDA UDI
Class IActive
Precolumn Cartridge 18068
FDA UDI
Class IActive
HPLC Column 46110/HR
FDA UDI
Class IActive
Precolumn Cartridge 18031
FDA UDI
Class IActive
Serum Control 0343
FDA UDI
Class IActive
Urine Control 0047
FDA UDI
Class IActive
Accessorie 65757
FDA UDI
Class IUnknown
Plasma Calibrator Set 92051/XT
FDA UDI
Class IIActive
Serum Calibration Standard 21003
FDA UDI
Class IIActive
Accessorie 81058
FDA UDI
Class IActive
Plasma Control 0072
FDA UDI
Class IActive
Urine Calibration Standard 4009
FDA UDI
Class IIActive
Reagent Kit 80800/96
FDA UDI
Class IActive
Reagent 34906
FDA UDI
Class IActive
Pasma Control 0315
FDA UDI
Class IActive
Reagent Kit 1000-C
FDA UDI
Class IActive
Accessorie 65759
FDA UDI
Class IUnknown
Plasma Control 0265
FDA UDI
Class IActive
Plasma Calibration Standard 67003
FDA UDI
Class IIActive
Reagent 2099
FDA UDI
Class IActive
Precolumn Cartridge 18052
FDA UDI
Class IActive
HPLC Column 67100
FDA UDI
Class IActive
HPLC Column 5100
FDA UDI
Class IActive
Plasma Control 0386
FDA UDI
Class IActive
Plasma Control Bi-Level 0230/XT
FDA UDI
Class IActive
Urine Control 0140
FDA UDI
Class IActive
Precolumn Cartridge 18043
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