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MESI d.o.o.

US

Last updated May 31, 2026

Part of Mesi D.o.o.

What MESI d.o.o. makes

MESI d.o.o. manufactures portable, multichannel electrocardiograph devices designed for professional use, including models with trauma brain injury (TBI) and ankle-brachial pressure index (ABI) capabilities. Their portfolio also includes noninvasive ankle-brachial pressure index measurement units and automatic-inflation electronic sphygmomanometers for finger-based blood pressure monitoring. Additional products extend ECG functionality, such as the BANANA AHA-compliant extension for the mTABLET ECG.

The company’s devices are classified under Class II regulatory standards and are listed in the FDA’s Unique Device Identifier (UDI) database. MESI d.o.o. operates from the United States, adhering to applicable medical device regulations for these categories.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
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Phone
+38616203487
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
500719478

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
MESI mTABLET ECG MTABSYSECG
FDA UDI
Class IIActive
MESI mTABLET TBI MTABSYSTBI
FDA UDI
Class IIActive
MESI mTABLET ABI MTABSYSABI
FDA UDI
Class IIActive
Mesi Abpi Md ABPIMDD
FDA UDI
Class IIActive
MESI mTABLET ECG Extension, BANANA AHA ECGSYSCS4 EN, BANANA AHA
FDA UDI
Class IIActive

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