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PeriWatch Surveillance

PERIGEN INC. · Model 2025.1.000 · UDI-DI 00860003483565

HGM Prescription
1
510(k) clearances
1,199
Adverse events (195 deaths)
28
Recalls
55
Facilities

Description

PeriWatch Surveillance is intended to be used as a complete Obstetrical Data Management System, which has the ability to record, store, and display data from fetal and maternal vital signs monitors. It manages patient information from the initial prenatal care to post-delivery discharge. It organizes clinical data that would normally be provided on paper records or other clinical systems and devices. The system also serves as a decision support tool and electronic medical record.

Recalls

DateFirmReason
2026-05-26Philips North America LlcMonitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of spe
2026-05-26Philips North America LlcMonitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of spe
2025-10-24Edan DiagnosticsAs a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
2025-10-24Edan DiagnosticsAs a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
2025-10-24Edan DiagnosticsAs a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
2024-05-22Philips North America LlcPotential for inaccurate fetal heart rate measurements when monitoring multiples.
2019-09-19Pacific Medical Group Inc.Fetal transducers distributed in advance of receiving 510(k) and international clearances.
2019-09-19Pacific Medical Group Inc.Fetal transducers distributed in advance of receiving 510(k) and international clearances.
2019-09-19Pacific Medical Group Inc.Fetal transducers distributed in advance of receiving 510(k) and international clearances.
2019-09-19Pacific Medical Group Inc.Fetal transducers distributed in advance of receiving 510(k) and international clearances.

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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.