M DIALYSIS INC.
US Last updated 27 May 2026 Part of M Dialysis AB
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- Devices
- 21
- Registries
- GUDID
- FDA recalls
- 0
Catalogue
Microvial rack 12/pkg Ref Rack
Perfusion fluid CNS Ref CNS
Pyruvate reagent 5 x Reagent, 5 x Buffer Ref 5 x Reagent, 5 x Buffer
Reagent Kit Ref Reagent
Rinsing Fluid 0.5 L 8/pkg Ref Rinsing Fluid
L-P-G Reagent kit Ref Reagent
MD Pump Kit, Brain Tissue CNS Ref CNS
Reagent Set C Ref Reagent
Reagent Set A Ref Reagent
Control Samples US 5 x Low, 5 x Elevated Ref 5 x Low, 5 x Elevated
70 Microdialysis Bolt Catheter 130/10, 4/pkg Ref 130/10
Calibrator A Ref Calibrator
Reagent Set B Ref Reagent
Glutamate reagent 5 x Reagent, 5 x Buffer Ref 5 x Reagent, 5 x Buffer
Battery 2x3V, 106 MD Pump Ref 106
Glucose reagent 5 x Reagent, 5 x Buffer Ref 5 x Reagent, 5 x Buffer
Glycerol reagent 5 x Reagent, 5 x Buffer Ref 5 x Reagent, 5 x Buffer
Lactate reagent 5 x Reagent, 5 x Buffer Ref 5 x Reagent, 5 x Buffer
ICUpilot Software eng English Ref English
What M DIALYSIS INC. makes
M Dialysis Inc. manufactures microdialysis systems, including perfusion fluids, reagents, and consumables such as catheters, microvial racks, and rinsing fluids. Their portfolio also includes bedside information systems designed to support real-time monitoring and analysis of microdialysis data, alongside specialized reagent kits and control samples for clinical use. The company produces components like perfusion fluids for central nervous system applications and pump kits tailored for brain tissue monitoring.
The company’s devices are classified under FDA’s Class I and Class II categories, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in microdialysis procedures, including diagnostic and research applications. The manufacturer operates from the United States, adhering to applicable regulatory requirements for medical devices in that jurisdiction.
Information
- Country
- US
- DUNS number
- 824632087