eOAE Portable Otoacoustic Emissions (OAE) Device for Newborn Hearing Screening

The eOAE is a portable otoacoustic emissions (OAE) device from BioMed Jena (Germany). It measures both transient-evoked otoacoustic emissions (TEOAE) and distortion-product otoacoustic emissions (DPOAE), and it includes a dedicated newborn hearing screening mode based on TEOAE. It weighs 320 g and has a 5-inch touchscreen. OAE testing is one of the standard methods used in newborn hearing screening programs.

iHear is the authorized distributor of BioMed Jena devices in the UAE. Headquartered in Al Ain, iHear offers the eOAE with technical support, training, and maintenance.

Quick Summary:

The eOAE is a portable German otoacoustic emissions device for TEOAE and DPOAE testing, with a dedicated newborn hearing screening mode. It has a 5-inch touchscreen, a replaceable battery, and a listed standard of DIN EN 60645-6:2010. It is available in the UAE through iHear.

eOAE otoacoustic emissions device key specifications
Field Details
Device name eOAE
Manufacturer BioMed Jena GmbH, Germany
Main use Otoacoustic emissions testing, including newborn hearing screening with a dedicated screening mode (TEOAE method)
Test principle Measurement of transient-evoked (TEOAE) and distortion-product (DPOAE) otoacoustic emissions: a very quiet sound sent back from the inner ear in response to an acoustic signal
Test settings 4 configurable profiles each for TEOAE and DPOAE; custom stopping criteria for TEOAE
Device type Portable; 5-inch TFT capacitive touchscreen; replaceable Li-ion battery (3.8 V, 3880 mAh); charging by docking station
Weight / dimensions 320 g / 141 × 97 × 27 mm
Standard listed in the datasheet DIN EN 60645-6:2010 (instruments for the measurement of otoacoustic emissions)
Distributor in the UAE iHear, Al Ain, UAE

What Is Otoacoustic Emissions (OAE) Testing, and How Does It Work?

Otoacoustic emissions (OAEs) are very faint sounds that a healthy inner ear (cochlea) sends back in response to sound. In an OAE test, a small probe placed in the ear canal plays soft sounds, and a sensitive microphone in the probe picks up the emission. The test does not require the person to respond, so it can be used with newborns and young children. It is often done while the baby is asleep or quiet, and it usually takes only a few minutes.

Two Types of Otoacoustic Emissions: TEOAE and DPOAE

TEOAE (transient-evoked otoacoustic emissions): the ear's response to brief clicks is measured. TEOAE is widely used in newborn hearing screening because the test is quick and simple, and it is the method of the eOAE's newborn screening mode. The eOAE's TEOAE range is 1–4 kHz.

DPOAE (distortion-product otoacoustic emissions): the ear's response to two pure tones of different frequencies played at the same time is measured. DPOAE gives frequency-specific information, which is useful for more detailed assessment and follow-up. The eOAE's DPOAE range is 0.5–8 kHz.

EOAE Portable Otoacoustic Emissions (OAE) Device for Newborn Hearing Screening

The eOAE supports both TEOAE and DPOAE in one device, so a clinic or hospital can use TEOAE for newborn screening and DPOAE for more detailed, frequency-specific assessment, depending on clinical need.

Newborn Hearing Screening in the UAE and the Role of the eOAE

Hearing screening is part of the UAE’s national newborn screening program. MoHAP’s National Newborn Screening Guidelines (July 2024) cover hearing screening in government and private hospitals, and Abu Dhabi’s Department of Health (DOH) lists it as a mandatory element of newborn screening, alongside the heel-prick test and pulse oximetry screening for heart defects. It is meant to be completed before the baby leaves the hospital.

OAE testing is non-invasive. A small probe in the baby’s ear canal plays soft sounds and records the faint echo that a healthy cochlea sends back, usually within a few minutes and often while the baby sleeps.

Finding hearing loss early, before a baby is six months old, gives the child a better chance of developing speech, language, and social skills. That is why maternity facilities that offer newborn hearing screening need suitable equipment, such as an OAE device.

Newborn hearing screening is a preventive check done in the first days of life. Finding hearing loss early, before a baby is six months old, gives the child a better chance of developing speech, language, and cognitive skills, because support can start sooner.

In the UAE, newborn screening is carried out in government and private health facilities. According to MoHAP reports cited by the Abu Dhabi Public Health Centre, uptake of newborn screening in Abu Dhabi reached 98% in 2021. The program covers a physical examination, hearing screening, critical congenital heart disease screening, and the heel-prick test. Facilities that offer newborn hearing screening need suitable equipment, such as an OAE device like the eOAE.

A small probe placed in the baby's ear canal plays a brief click (TEOAE) or two tones at once (DPOAE). A healthy cochlea responds with a very faint echo, which a sensitive microphone picks up. The eOAE analyzes the response and shows it on its touchscreen as a clear chart. The test does not need sedation, and a quiet or sleeping baby makes it easier to record a clean result.

The eOAE measures two types of emissions:

  • TEOAE (transient-evoked): widely used in newborn hearing screening because the test is quick and simple, and it is the method of the eOAE's newborn screening mode.
  • DPOAE (distortion-product): covers a wider frequency range (0.5–8 kHz) when further assessment is needed.

No. Newborn hearing screening programs use OAE, automated auditory brainstem response (AABR), or both. Babies who do not pass the screening, or who have risk factors, are referred for further testing, which includes ABR. OAE tests the function of the cochlea, so a normal OAE result does not rule out hearing loss further along the hearing pathway, such as auditory neuropathy. For this reason, some programs use AABR for babies who have been in intensive care.

A facility starting a newborn hearing screening service can begin with an OAE device such as the eOAE. BioMed Jena's eABR USB covers ABR testing, and iHear supplies both. The choice of protocol follows the facility's program and the clinician's judgment.

The eOAE includes a dedicated screening mode for newborn examinations, based on the TEOAE method, with a clear chart illustration of the result. Decisions about referral and follow-up remain with the clinician and follow the facility's screening protocol.

eOAE Key Features for Newborn Hearing Screening

01

Newborn screening mode: a dedicated mode for newborn examinations using the TEOAE method, with a clear chart illustration of the result.

02

TEOAE and DPOAE: both emission types are measured in one device, with 4 configurable profiles for each and custom stopping criteria for TEOAE.

03

Portable touchscreen device: a 5-inch capacitive touchscreen, 320 g, with patient registration and data management on the device itself.

04

Replaceable battery and docking station: a replaceable Li-ion battery (3880 mAh), with charging and data synchronization when the device is placed in the docking station.

05

eDM and GDT integration: full integration with the eDM Diagnostic Manager, plus a GDT interface to connect results to a clinic or hospital system.

06

Automatic reports: the eOAE PC software generates reports automatically and can store results as PDF files.

07

Optional thermal printer: printing of results with an optional thermal printer connected through the docking station.

08

Easy cleaning: the probe parts are easy to clean, and the touchscreen is easy to sanitize between patients. Optional masking headphones (IP30 or DD45) are available.

09

Made in Germany: the datasheet lists the standard DIN EN 60645-6:2010 and the CE 0124 mark (Class IIa according to MDD).

EOAE Key Features for Newborn Hearing Screening

Who Is the eOAE Newborn Hearing Screening Device For?

Hospitals and maternity centers

Facilities that take part in the UAE's national newborn screening program (MoHAP guidelines and, in Abu Dhabi, Department of Health standards), where hearing screening is part of newborn care.

Neonatal care units

Neonatal intensive care units (NICU) that want a portable device for use at the bedside. Many programs add or use AABR for babies who have been in intensive care, so confirm your unit's protocol.

Private clinics

Pediatric clinics and audiologists who want to offer early hearing screening as part of their services.

Screening and health centers

Medical examination centers (public and private) that run infant and child hearing screening. OAE is one tool among others, and older children are often tested with pure-tone audiometry.

Audiology centers

Audiology centers that want OAE testing alongside other tests. The eOAE adds otoacoustic emissions testing, and it can sit in the same eDM patient database as BioMed Jena's audiometer (eAUDIO USB), middle-ear analyzer (eTYMP USB), and ABR device (eABR USB).

How Does the eOAE Work in Newborn Hearing Screening?

01

A small, lightweight probe is placed in the baby's ear canal. (OAE testing is non-invasive.)

02

The device plays soft sounds (clicks for TEOAE, tones for DPOAE) and records the faint echo that a healthy cochlea sends back.

03

The device displays the result as a clear chart on its touchscreen.

04

A "refer" screening result does not necessarily mean permanent hearing loss (fluid in the middle ear, for example, can cause one). The usual approach is to retest, and if the result is repeated, the baby is referred for further testing such as ABR, which BioMed Jena's eABR USB measures. The clinician decides on follow-up.

The eOAE's newborn screening mode uses the TEOAE method and shows the result as a clear chart. Newborn hearing screening should be performed by trained healthcare personnel, following your facility's protocol.

How Does the eOAE Work in Newborn Hearing Screening 1024x683

eOAE Technical Specifications

eOAE Device Specifications

SpecificationValue
Measurement typeTEOAE and DPOAE
Screen5-inch TFT with capacitive touch
Weight320 g
Dimensions141 × 97 × 27 mm (L × W × H)
BatteryReplaceable Li-ion battery, 3.8 V, 3880 mAh
Protection classClass II (EN 60601-1)
Degree of protectionType BF
Protection typeIPX0 (no protection against liquid ingress)
ChargingDocking station with spring contacts
KeyboardQwerty keyboard on the device
Masking headphonesIP30 or DD45 (optional)
Standard listed in the datasheetDIN EN 60645-6:2010

Regulatory Information

ItemValue
Medical device classificationClass IIa according to the Medical Device Directive (MDD)
CE markingCE 0124
The four-digit number after the CE mark identifies the notified body involved in the conformity assessment. CE marking is a European conformity marking, and use in the UAE is subject to the requirements of the relevant UAE health authority, so ask iHear for the current status.

Power Supply Specifications

SpecificationValue
ModelACM18US05
Input90–264 VAC, 47–63 Hz
Power consumption48 W maximum
Output5 VDC, up to 2.5 A

Probe Specifications

SpecificationValue
Measurement typeTEOAE and DPOAE
TEOAE stimulusNonlinear clicks, 100 µs width, 20 µs rise and fall time
DPOAE stimulusTwo primary sinusoidal tones (phase-aligned), frequency ratio f1:f2 = 1:1.2
TEOAE frequency range1–4 kHz
DPOAE frequency range0.5–8 kHz
TEOAE stimulus level40–90 dB peSPL
DPOAE stimulus level40–70 dB SPL
Cable length1.5 m

PC Requirements for the eOAE Software

RequirementSpecification
Operating systemWindows 10
ProcessorIntel i3, 2 GHz
RAM4 GB
Screen resolution1920 × 1080
These values are taken from the eOAE datasheet. Ask iHear to confirm the requirements for the software version you will receive.

Optional Thermal Printer

SpecificationValue
TypeThermal printer
Speed50–80 mm/s
PaperThermal paper, 57.5 mm wide, roll diameter up to 39 mm
Resolution8 dots/mm, 384 dots/line
ConnectionThrough the docking station

Ports

  • Port for power supply
  • USB Type-C port
  • Port for the probe
  • Spring contacts for the docking station
  • Port for the optional printer

Environmental Conditions

ConditionTemperatureHumidityNotes
Transport−10 to 50 °C5%–90%, no condensationAt 700–1060 hPa air pressure
Operation+10 to 40 °C5%–80%, no condensationAt 700–1060 hPa air pressure
Periodic safety checks (STC): the datasheet states that periodic safety checks are to be carried out according to chapter 10.1 of the user manual.

Newborn Screening Mode and Software Features

  • Dedicated newborn screening mode using the TEOAE method, with a clear chart illustration.
  • 4 configurable profiles each for TEOAE and DPOAE.
  • Custom stopping criteria for TEOAE.
  • Results shown as a time graph or frequency diagram (TEOAE) and as a DP-gram and chart (DPOAE).
  • Full integration with the eDM Diagnostic Manager, plus a GDT interface for connecting results to a clinic or hospital system.
  • Patient registration on the device or on the PC, with data synchronization when the device is placed in the docking station.
  • Automatic report generation, with results stored as PDF files.
  • Easy cleaning of the probe parts and good sanitizability of the touchscreen.

eOAE vs. Other Portable Newborn Hearing Screening Devices

This category of devices (portable OAE screeners for newborn hearing screening) has different competitors from the large evoked-response platforms. Here is a detailed comparison based on the officially published specifications of the leading competitors on the market:

MAICO EroScan

Country of origin: United States (Etymotic)
  • Supported testsTEOAE and/or DPOAE
  • ScreenOLED screen (no touch)
  • Data entryLimited on the device itself
  • Storage capacityNot explicitly stated in the sources
  • ABR moduleNo
  • Diagnostic integrationMAICO's own software / NOAH

Otodynamics Otoport

Country of origin: United Kingdom
  • Supported testsTEOAE and/or DPOAE (depending on the model)
  • ScreenSmall screen (simple interface)
  • Data entryLimited, depends on PC software
  • Storage capacityUp to 500 (Lite) or 5,000 (Screener)
  • ABR moduleYes: optional sleeve (ABR Sleeve)
  • Diagnostic integrationOtolink's own software

GSI Novus

Country of origin: United States
  • Supported testsComprehensive screening (OAE and sometimes ABR)
  • ScreenModern portable design
  • Data entryDepends on a companion app
  • Storage capacityNot explicitly stated
  • ABR moduleYes: combines OAE and ABR together
  • Diagnostic integrationGSI's own software

An Honest Summary of the Comparison

If your top priority is combining OAE and ABR screening in one portable device, some Otodynamics and GSI Novus models offer that combination directly. If your priority is a large touchscreen that is easy for the nursing team, direct data entry on the device without a computer, and full integration with a broader diagnostic system (tympanometry, audiometry, and evoked responses) from the same company through a single database, then the eOAE with the rest of the BioMed Jena family offers strong value for an integrated diagnostic center, not just a standalone device.

eOAE and the BioMed Jena Device Family: Why Integration Matters

The eOAE is not a standalone tool. It is part of a family of diagnostic devices from BioMed Jena, which iHear supplies in the UAE:

eOAE + eTYMP USB

Combination 1

To check middle-ear function (tympanometry) before interpreting OAE results, since middle-ear problems can affect OAE.

eOAE + eABR USB

Combination 2

For further testing of newborns who do not pass the initial OAE screening, and when auditory neuropathy is a concern.

eOAE + eAUDIO USB

Combination 3

To build a fuller hearing picture that combines objective assessment (OAE) with behavioral assessment (pure-tone audiometry) for older patients.

eDM (Diagnostic Manager)

The central software

BioMed Jena's data management software. The eOAE datasheet lists full integration with eDM, automatic PDF reports, and a GDT interface for connecting results to hospital systems. BioMed Jena describes eDM as one software for all of its devices, with a single patient database.

Buy the eOAE Newborn Hearing Screening Device in the UAE From iHear

Authorized distributor of BioMed Jena devices (Germany) in the UAE.
Technical support and training for your team on using the device and the eDM software.
Maintenance support, including the periodic safety checks listed in the datasheet.
Spare parts and warranty support. Ask iHear for the terms that apply to your purchase.
Headquartered in Al Ain, serving clinics and medical centers.
A branch in Abu Dhabi serving the medical sector.
📍 Al Ain Branch: Al Humaira, 136 Khalifa Bin Zayed Street, Mezzanine 2, Office 3
📍 Abu Dhabi Branch: Sultan Bin Zayed The First Street (Muroor Road), Building 1210, Offices M6
☎ Al Ain phone: +971 3 768 5563
☎ Abu Dhabi phone: +971 2 681 3841
📧 Email: Info@ihear.ae
📱 WhatsApp: +971 50 208 4569

📞 Contact the iHear team in Al Ain or Abu Dhabi to request an audiometer quote for your clinic on WhatsApp

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Other BioMed Jena Devices for Your Clinic

BioMed Jena devices related to the eOAE
Device Use Relationship to the eOAE
eABR USB Auditory brainstem response (ABR / BERA) measurement Often used for further testing of babies who do not pass the OAE screening, and for babies with risk factors; the clinician decides
eAUDIO USB 2-channel diagnostic audiometer (pure-tone and speech audiometry) For behavioral hearing testing once a child is old enough to cooperate
eTYMP USB Middle-ear analyzer (tympanometry) A complementary test when a middle-ear problem is suspected, since middle-ear problems can affect OAE results

eOAE FAQ: Common Questions About Newborn Hearing Screening and OAE Testing

The eOAE is a portable otoacoustic emissions (OAE) device from BioMed Jena (Germany). It measures transient-evoked (TEOAE) and distortion-product (DPOAE) otoacoustic emissions, and it includes a dedicated newborn hearing screening mode. It weighs 320 g and has a 5-inch touchscreen. OAEs are very faint sounds that a healthy inner ear (cochlea) sends back in response to sound.

iHear (ihear.ae) is the authorized distributor of BioMed Jena devices in the UAE, headquartered in Al Ain with a branch in Abu Dhabi. To request a quote or a consultation, contact iHear on WhatsApp at +971 50 208 4569.

The price depends on the configuration, for example whether you add the optional thermal printer or masking headphones. Contact iHear for a quote based on your facility's needs.

Hearing screening is part of the UAE's national newborn screening program. The Ministry of Health and Prevention (MoHAP) launched National Newborn Screening Guidelines in July 2024 that cover hearing and heart screening in government and private hospitals, and Abu Dhabi's Department of Health (DOH) newborn screening standards list hearing screening as a mandatory element. Screening is meant to be completed before the baby leaves the hospital. Requirements in other emirates may differ, so confirm what applies to your facility.

An Abu Dhabi DOH program document describes the initial newborn hearing screening as preferably done 12 hours or more after birth by trained healthcare personnel, and early hearing detection programs aim to screen every newborn before hospital discharge. The widely cited 1-3-6 benchmark aims for screening by 1 month of age, diagnosis by 3 months, and early intervention by 6 months. Follow your facility's protocol and current health authority guidance.

An OAE test checks the function of the inner ear (cochlea). A small probe placed in the ear canal plays soft sounds, and a sensitive microphone picks up the faint echo that a healthy cochlea sends back. The test is non-invasive and does not require the person to respond, so it can be used with newborns, often while the baby is asleep or quiet. A noisy room, a restless baby, or fluid or debris in the ear can affect the result.

TEOAE measures the ear's response to brief clicks. DPOAE measures the response to two pure tones of different frequencies played at the same time (a frequency ratio of f1:f2 = 1:1.2 on the eOAE). TEOAE is widely used in newborn hearing screening because the test is quick and simple, while DPOAE gives frequency-specific information that is useful for more detailed assessment. The eOAE measures both.

Universal newborn hearing screening programs screen all newborns, not only babies with risk factors, because many babies with hearing loss have no known risk factor. Finding hearing loss early gives a child a better chance of developing speech, language, and social skills.

A "refer" (did not pass) screening result does not necessarily mean permanent hearing loss, because fluid or debris in the ear can cause it. The usual approach is to retest, and if the result is repeated, the baby is referred for further testing such as ABR. The clinician decides on follow-up.

Yes. OAE reflects the function of the cochlea, so a normal result does not rule out a problem further along the hearing pathway, such as auditory neuropathy spectrum disorder (ANSD), where the cochlea works normally but signals reach the brain poorly. That is why many programs use ABR or AABR for some babies, for example those who have been in intensive care, and why a baby who passes OAE but does not respond to sounds still needs assessment.

The eOAE tests the function of the cochlea. The eABR USB measures the auditory brainstem response (ABR), which assesses the hearing pathway up to the brainstem, so it is often used for further testing, for example when a baby does not pass the OAE screening or has risk factors. The choice of test follows the facility's protocol and the clinician's judgment.

BioMed Jena's company history lists the development of a new AABR/ABR module for the eOAE in 2023, but the eOAE datasheet does not describe this function. ABR testing is available separately with the eABR USB. Contact iHear to confirm the current eOAE configuration.

No. The eOAE has a newborn screening mode, but OAE testing can be used at other ages because it does not need the patient to respond. BioMed Jena's 2025/2026 catalogue also lists a screening pure-tone audiometry function with DD65V2 headphones (125 Hz to 8 kHz at up to 100 dB HL). Screening pure-tone audiometry is not a full diagnostic hearing test; for that, see the eAUDIO USB audiometer.

The eOAE is a handheld device with a touchscreen and a keyboard, and measurement data can be managed on the device itself. Patients can be registered on the device or on the PC, and data synchronizes when the device is placed in its docking station. The PC software adds report generation, PDF export, and eDM integration, and BioMed Jena lists it for remote operation.

The eOAE has a replaceable Li-ion battery (3.8 V, 3880 mAh). BioMed Jena's 2025/2026 catalogue lists a minimum of 400 tests per charge. The device charges and synchronizes data in its docking station.

BioMed Jena's 2025/2026 catalogue lists a capacity of 10,000 tests on the eOAE. Results can be managed on the device, saved automatically as PDF reports, sent to hospital systems through a GDT interface, and printed with the optional thermal printer. The eDM software adds a single patient database.

According to the eOAE datasheet: a 5-inch capacitive touchscreen, 320 g, 141 x 97 x 27 mm, a replaceable 3.8 V 3880 mAh Li-ion battery, and a docking station. The TEOAE stimulus is nonlinear clicks (1 to 4 kHz, 40 to 90 dB peSPL), the DPOAE stimulus is two pure tones (f1:f2 = 1:1.2, 40 to 70 dB SPL), and the probe cable is 1.5 m. Protection class II, Type BF, IPX0 (no protection against liquid ingress). An optional thermal printer and optional masking headphones are available.

Yes. eDM (Diagnostic Manager) is BioMed Jena's software for all of its devices, with a single patient database. BioMed Jena's catalogue lists the eOAE in eDM together with the eAUDIO USB, eTYMP USB, eABR USB, and its vestibular devices such as the eVNG and eHIT. eDM includes a GDT interface (HL7 on request) and exports PDF reports automatically.

A program typically needs a screening device (an OAE device such as the eOAE, or an AABR device), suitable ear tips, a way to record and export results, trained staff, and equipment for follow-up testing, such as ABR and tympanometry to check the middle ear. BioMed Jena's eABR USB and eTYMP USB cover ABR and tympanometry. The right set depends on your protocol and patient volume, so contact iHear to plan it.

When comparing portable OAE devices, check which emission types are measured (TEOAE, DPOAE, or both), the newborn screening mode and how results are displayed, the display and data entry, weight and battery life, data management and export options (PDF, GDT, HL7), whether a printer is available, how follow-up ABR or AABR testing is handled, the standards and regulatory status, and local training and support. For the eOAE, the datasheet lists TEOAE and DPOAE, a newborn screening mode, a 5-inch touchscreen, 320 g, a replaceable 3880 mAh battery, PDF reports, a GDT interface, eDM integration, and DIN EN 60645-6:2010. Contact iHear to discuss which device fits your program.

The national program covers newborn hearing screening, and Abu Dhabi DOH documents describe OAE as a screening method. The eOAE is an OAE device with a dedicated newborn screening mode. Whether it meets a particular facility's or program's requirements, including its regulatory status in the UAE, should be confirmed with your health authority. iHear can provide the datasheet and documents.

The eOAE datasheet lists Class IIa according to the Medical Device Directive (MDD), the CE 0124 mark, and the standard DIN EN 60645-6:2010. CE marking is a European conformity marking, and use in the UAE is subject to the requirements of the relevant UAE health authority, so ask iHear for the current status and documents for your facility.

OAE is not a substitute for pure-tone audiometry in occupational programs. In Abu Dhabi, the ADOSH-SF Occupational Noise Code of Practice (CoP 3.0) requires pure-tone air conduction threshold audiometry for employees exposed to 85 dB(A) or more, using audiometers that meet ANSI S3.6-2010 or ISO 8253-1:2010. For pure-tone testing, BioMed Jena's audiometer is the eAUDIO USB; ask iHear whether it meets your program's requirements.

iHear offers technical support, training, and maintenance for the eOAE in the UAE. Warranty and spare-part terms are set in your purchase documents, so ask iHear what applies to your purchase. The eOAE datasheet also lists periodic safety checks (STC) according to chapter 10.1 of the user manual.
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