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Midmark IQholter® Digital Holter Recorder

MIDMARK CORPORATION · Model 1-370-0005 · UDI-DI 00841709100659

MLO Prescription
10
510(k) clearances
23
Adverse events (2 deaths)
2
Recalls
31
Facilities

Description

Small and lightweight digital Holter recorder. Standard 24-hour recording with 48 and 72-hour recording capabilities available.

Recalls

DateFirmReason
2024-10-11Baxter Healthcare CorporationThere is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System
2024-10-11Baxter Healthcare CorporationThere is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.