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Monitor, St Segment With Alarm
FDA product code MLD · Class 2 · Cardiovascular
239
Registered devices
33
Adverse events
2
Recalls
14
510(k) clearances
Devices with this code
Welch Allyn, Inc. — WELCH ALLYN, INC.CARESCAPE B850 — GE Healthcare Finland OyVital Signs — Carefusion Finland 320 OyPatient Monitor — Edan Instruments, Inc.RespArray — Edan Instruments, Inc.Vital Signs — Carefusion Finland 320 OyVital Signs — Carefusion Finland 320 OyVital Signs — Carefusion Finland 320 OyWelch Allyn, Inc. — WELCH ALLYN, INC.LIFEE — Caf Medical Solutions, IncXHIBIT — SPACELABS HEALTHCARE (WASHINGTON), INCCare Assist — Philips Medical Systems HsgPatient Monitor — Edan Instruments, Inc.Welch Allyn, Inc. — WELCH ALLYN, INC.NA — GE Healthcare Finland OyVital Signs — Carefusion Finland 320 OyADVANCED PATIENT MONITOR — ADVANCED INSTRUMENTATIONS, INC.VectraplexECG System — VECTRACOR INCCare Assist — Philips Medizin Systeme Böblingen GmbHVital Signs — Carefusion Finland 320 OyXhibit — SPACELABS HEALTHCARE (WASHINGTON), INCNA — GE Medical Systems Information Technologies, Inc.Patient Monitor — Edan Instruments, Inc.Patient Monitor — Edan Instruments, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-02-06 | GE Medical Systems Information Tecnology | GE Healthcare (Datex-Ohmeda) S/5 Critical Care Monitor and S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software had an issue |
| 2006-02-06 | GE Medical Systems Information Tecnology | GE Healthcare (Datex-Ohmeda) S/5 Critical Care Monitor and S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software had an issue |
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