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Monitor, St Segment With Alarm
FDA product code MLD · Class 2 · Cardiovascular
244
Registered devices
33
Adverse events
2
Recalls
14
510(k) clearances
Devices with this code
Vital Signs — Carefusion Finland 320 OyNA — GE Medical Systems Information Technologies, Inc.Vital Signs — Carefusion Finland 320 OyCARESCAPE B450 — GE Healthcare Finland OyVital Signs — Carefusion Finland 320 OyCare Assist — Philips Medizin Systeme Böblingen GmbHWelch Allyn, Inc. — WELCH ALLYN, INC.Welch Allyn, Inc. — WELCH ALLYN, INC.NA — GE Healthcare Finland OyWelch Allyn, Inc. — WELCH ALLYN, INC.Care Assist — Philips Medizin Systeme Böblingen GmbHPatient Monitor — Edan Instruments, Inc.NA — GE Healthcare Finland OyPatient Monitor — Edan Instruments, Inc.ADVANCED PATIENT MONITOR — ADVANCED INSTRUMENTATIONS, INC.Patient Monitor — Edan Instruments, Inc.Care Assist — Philips Medizin Systeme Böblingen GmbHCare Assist — Philips Medizin Systeme Böblingen GmbHWelch Allyn, Inc. — WELCH ALLYN, INC.NA — GE Medical Systems Information Technologies, Inc.Waveline EZ-MAX — AvanteCARESCAPE — GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.CARESCAPE — GE Healthcare Finland OyXhibit Telemetry Receiver — SPACELABS HEALTHCARE (WASHINGTON), 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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