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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 9 of 12
DeviceModel / ReferenceRegistriesClassStatus
Reagent 80676
FDA UDI
Class IActive
Reagent Kit 80700/C
FDA UDI
Class IActive
Plasma Control Bi-Level 0249/XT
FDA UDI
Class IActive
Reagent 34001
FDA UDI
Class IActive
Serum Control 0311
FDA UDI
Class IActive
Plasma Control 0250/XT
FDA UDI
Class IActive
Whole Blood Control Bi-Level 0164
FDA UDI
Class IActive
Reagent Kit 34934/UHPLC
FDA UDI
Class IActive
Urine Control 0367
FDA UDI
Class IActive
Reagent 2029/COMBI
FDA UDI
Class IActive
Reagent Kit 34700/F
FDA UDI
Class IActive
Analytical Column 62100
FDA UDI
Class IActive
Urine Control Bi-Level 0141
FDA UDI
Class IActive
Precolumn Cartridge 18024
FDA UDI
Class IActive
Reagent 32005
FDA UDI
Class IActive
Precolumn Cartridge 18038
FDA UDI
Class IActive
Urine Calibrator Set 75228
FDA UDI
Class IIActive
Reagent 34003
FDA UDI
Class IActive
Plasma Control Bi-Level 0051
FDA UDI
Class IActive
HPLC Column 35110
FDA UDI
Class IActive
Urine Calibrator Set 69039
FDA UDI
Class IIActive
Serum Control 0256
FDA UDI
Class IActive
Plasma Control Bi-Level 0249-XT2
FDA UDI
Class IActive
Plasma Control 0095
FDA UDI
Class IActive
Plasma Calibrator Set 46029
FDA UDI
Class IIActive
Reagent Kit 2020-C
FDA UDI
Class IActive
Reagent 80703
FDA UDI
Class IActive
Plasma Control 0384
FDA UDI
Class IActive
Saliva Control 0353
FDA UDI
Class IActive
Serum Control 0222
FDA UDI
Class IActive
Reagent 1013/A5
FDA UDI
Class IActive
HPLC Column 32100
FDA UDI
Class IActive
Reagent 1006/A
FDA UDI
Class IActive
Plasma Control 0471
FDA UDI
Class IActive
Reagent 6033
FDA UDI
Class IActive
Reagent Kit 80000
FDA UDI
Class IActive
HPLC Column 24100
FDA UDI
Class IActive
Calibration Standard 1003/B
FDA UDI
Class IIActive
Reagent 6006/A
FDA UDI
Class IActive
Accessorie 34459
FDA UDI
Class IActive
Serum Calibration Standard 24003
FDA UDI
Class IIActive
Basic Kit 2020-B-BK
FDA UDI
Class IActive
Restrictor Capillary 55015
FDA UDI
Class IActive
Reagent 2025/A1
FDA UDI
Class IActive
Plasma Control Bi-Level 0210/XT
FDA UDI
Class IUnknown
HPLC Column 6100
FDA UDI
Class IActive
Basic Kit 34400-DWP-BK
FDA UDI
Class IActive
Reagent 2025
FDA UDI
Class IActive
Plasma Control 0092
FDA UDI
Class IActive
Serum Calibrator Set 72038
FDA UDI
Class IIActive

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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