Meridian M110 Fetal Monitoring System

FDA UDI

Class II (US FDA UDI)

by Mindchild Medical

Identity

Trade Name: Meridian M110 Fetal Monitoring System FDA UDI
Generic Name: Foetal/maternal prenatal monitor FDA UDI
Device Name: The MERIDIAN M110 Fetal Monitoring System is an intrapartum fetal monitor that externally measures and displays fetal heart rate (FHR), maternal heart rate (MHR), and uterine contractions (UA). The MERIDIAN M110 Fetal Monitoring System acquires and displays the FHR and UA from abdominal surface electrodes that detect the fetal ECG signals, maternal ECG signals, and of uterine muscle contraction signals. FDA UDI
Model / Reference: M110 FDA UDI
Description: The MERIDIAN M110 Fetal Monitoring System is an intrapartum fetal monitor that externally measures and displays fetal heart rate (FHR), maternal heart rate (MHR), and uterine contractions (UA). The MERIDIAN M110 Fetal Monitoring System acquires and displays the FHR and UA from abdominal surface electrodes that detect the fetal ECG signals, maternal ECG signals, and of uterine muscle contraction signals. FDA UDI

Identifiers

Primary DI / UDI-DI: 00867696000307 FDA UDI
FDA Product Code: HGM FDA UDI
GMDN Term: Foetal/maternal prenatal monitor FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.2740 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Foetal/maternal prenatal monitor

Meridian M110 Fetal Monitoring System by Mindchild Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foetal/maternal prenatal monitor.

Cetro America Ultrasound Transducer 1.150MHz, for Sonomed with blue lemo conne — Cetro America · Class II
Cetro America Ultrasound Transducer for HP8040, Waterproof — Cetro America · Class II
Ameritus Transducer — KENTEC MEDICAL, INC. · Class II
OBIX — Huntleigh Healthcare , Ltd. · Class II
OBIX — Huntleigh Healthcare , Ltd. · Class II
Novii — Datex-Ohmeda Inc. · Class II
SONICAID — Huntleigh Healthcare , Ltd. · Class II
COROMETRICS 170 SERIES — Wipro GE Healthcare Private Ltd · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Mindchild Medical

Sources (1)

FDA UDI 6fafefae-b3b4-492d-915a-da7177abc697 33 fields · synced Jun 8, 2026