eABR USB: Portable ABR (BERA) System with Optional VEMP Testing

The eABR USB is a 2-channel auditory brainstem response (ABR) system from the German manufacturer BioMed Jena. About the size of a TV remote control (55 × 155 × 25 mm, just 140 g), it is still a full routine-use device for auditory evoked potentials. Unlike conventional audiometry, it does not depend on the patient's conscious response. It records the electrical response of the auditory nerve and brainstem to sound, which makes it an objective hearing test.

The eABR USB covers two distinct tests in one device:

- Auditory brainstem response (ABR/BERA) testing: assesses hearing in patients who cannot give a reliable behavioral response, above all newborns and infants.
- VEMP (vestibular evoked myogenic potentials) testing: assesses vestibular function in patients with dizziness and vertigo. It is available as an optional module (cVEMP and oVEMP).

iHear, the authorized distributor of BioMed Jena devices in the UAE, provides local technical support, training, and servicing from its branches in Al Ain and Abu Dhabi.

Specification Details
Model eABR USB (also written eABRUSB)
Manufacturer BioMed Jena GmbH, Germany (device developed in 2016)
Device type Portable auditory brainstem response (ABR/BERA) system, with optional VEMP testing for vestibular assessment
Test method Fully objective: no active response needed from the patient (works even while an infant sleeps)
Size and weight Remote-control sized: 55 × 155 × 25 mm, 140 g without accessories
Channels 2 channels (24-bit, 48 kHz)
Main uses (1) Objective hearing testing (ABR/BERA) for babies, infants and children
(2) VEMP testing to assess vestibular disorders (dizziness and balance)
Standards EN 60645-7:2010 / 93/42/EEC (Medical Device Directive)
Authorized distributor in the UAE iHear, Al Ain and Abu Dhabi, UAE

Quick summary: The eABR USB is a portable German auditory brainstem response (ABR/BERA) system, about the size of a remote control. ABR is the standard objective hearing test for newborns, infants and children who cannot respond to sounds on their own. An optional module adds cVEMP and oVEMP testing to help diagnose dizziness and vertigo. Complies with EN 60645-7:2010. Available in the UAE through iHear, the authorized distributor of BioMed Jena.

What Is the eABR USB, and How Does an ABR Test Differ from a Standard Hearing Test?

The eABR USB is an auditory brainstem response (ABR) system. ABR is also known as BERA (brainstem evoked response audiometry), the name many clinics use, and parents often just call it the “brainstem test” for babies. The device uses small electrodes placed on the head to record the electrical activity that the hearing nerve and brainstem produce in response to sound, with no active response needed from the patient. This sets it apart from the eAUDIO USB, where the patient has to press a button when they hear a tone, and even from the eTYMP USB, which only checks how the middle ear works mechanically. The eABR USB tests the actual neural pathway, from the inner ear all the way to the brainstem.

With an optional module, the same device also measures VEMP (vestibular evoked myogenic potentials). In this test, a loud sound triggers a response in the neck muscle (cVEMP) or in the muscles around the eyes (oVEMP). It serves a completely different purpose: assessing the saccule and utricle, the two otolith organs of the inner ear that control balance, not hearing.

What Is a BERA Test (Auditory Brainstem Response, ABR)?

BERA vs ABR: Same Test, Different Names

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Before going into detail, a quick clarification: BERA and ABR are, in practice, two names for the same test. "ABR" (Auditory Brainstem Response) is the technical term for the electrical signal itself, while "BERA" (Brainstem Evoked Response Audiometry) is the name that became common in everyday clinical use, especially in the Gulf, Egypt and South Asia, for using that same signal to estimate a person's hearing threshold.

You will see the two terms used interchangeably in many medical sources. Even the manufacturer of the eABR USB calls the hearing threshold protocol in its software "Threshold-BERA". You may also come across auditory evoked potentials (AEP), a broader term that covers ABR and other types of auditory evoked responses.

How Does an ABR (BERA) Test Work?

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The auditory brainstem response is a set of very small electrical signals that the hearing nerve and brainstem send automatically when they hear a sound (a click or a short tone). Small adhesive electrodes placed on the forehead and behind the ears record these signals. The patient does not need to take part at all, so the test can usually be done during a baby's natural sleep, without sedation.

The result appears as a series of waves (I to V) within the first 10 milliseconds after the sound. The clinician checks the timing of these waves and compares them between the two ears to assess the whole hearing pathway, from the inner ear to the brainstem.

When Is an ABR Test Needed?

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An ABR test is used mainly when a standard hearing test cannot give reliable results:

  • Newborns and infants who cannot raise a hand or signal when they hear a sound
  • Children from about 3 months to around 3 years old, the age range in which reliable behavioral audiometry is difficult
  • Asymmetric hearing loss between the two ears, or a suspected problem with the hearing nerve itself rather than only the inner ear, including initial screening for acoustic neuroma (vestibular schwannoma) before an MRI
  • Patients who cannot respond voluntarily, such as those with severe intellectual disability or in a coma

Accuracy note: ABR is also used in some advanced centers worldwide for continuous auditory nerve monitoring during acoustic neuroma removal surgery (intraoperative neuromonitoring). However, this is a highly specialized application that usually requires dedicated intraoperative monitoring platforms, and it is not an officially documented use of the eABR USB according to its published specifications. Mention it as background information if you wish, but do not market the device for this purpose without direct technical confirmation from BioMed Jena.

What Is the eABR USB, and How Does an ABR Test Differ from a Standard Hearing Test

eABR USB and Mandatory Newborn Hearing Screening in the UAE

Mandatory & Officially Approved

Newborn Hearing Screening Is Not Optional in the UAE

The UAE Cabinet has approved a newborn hearing screening program, enacted into official law as part of the comprehensive newborn medical screening system, alongside blood and heart screening tests. In practice, Emirates Health Services (EHS) publishes actual monthly compliance data. For example, compliance with newborn hearing screening in 2025 ranged between 96.3% and 99.1% per month, reflecting a serious, ongoing screening system rather than a temporary initiative.

Why This Matters If You're Considering the eABR USB

Newborn hearing screening is typically carried out in two internationally standard stages: an initial otoacoustic emissions (OAE) screening for all newborns, followed by a confirmatory auditory brainstem response (ABR/AABR) test for babies who do not pass the first stage or who have additional risk factors (low birth weight, premature birth, family history of hearing loss, infection during pregnancy). Any healthcare facility, whether a private hospital, pediatric clinic, or specialized screening center, that wants to offer both stages of this service needs both an OAE device and an ABR device. This is exactly what the BioMed Jena eOAE and eABR USB pair provides, within the same eDM system.

Signs That Call for an ABR Test Referral, Even After Passing the Initial Screening

  • Noticeable lack of response to sounds compared with other children the same age.
  • Clear delay in speech or language development.
  • Family history of hereditary sensorineural hearing loss.
  • Maternal infection during pregnancy (rubella, herpes, toxoplasmosis) or birth risk factors (low birth weight, premature birth, NICU stay).

eABR USB and VEMP Testing for Dizziness and Vertigo Clinics

Company Roots: BioMed Jena Started Out as a Vertigo Diagnostics Company

A detail worth noting: according to the company's official history, BioMed Jena did not begin with hearing test equipment. In 1998, only its second year after founding, it launched a Vertigo Diagnostic Line as an OEM developer and manufacturer, before later introducing its own brand with devices such as the eVNG. In other words, the company's expertise in balance and dizziness diagnostics is its founding foundation, not a later add-on to an audiology product line.

What Is a VEMP Test, and Why Do Dizziness Specialists Order It?

Vestibular evoked myogenic potentials (VEMP) is a test that evaluates the function of the saccule and utricle in the inner ear. These are part of the vestibular system, which is responsible for balance. The test works by recording an automatic muscle response to a loud sound or vibration. It differs from other vertigo tests, such as caloric testing or videonystagmography (VNG), because it specifically examines a different neural pathway (the inferior vestibular nerve), which makes it a complement to, not a replacement for, other balance tests.

A VEMP test is commonly requested as part of the evaluation of:

  • Meniere's disease and monitoring its progression
  • Vestibular neuritis and distinguishing it from other causes of vertigo
  • Superior semicircular canal dehiscence (SCDS), where VEMP is a key diagnostic tool
  • Comprehensive assessment before certain inner ear surgeries

Why the eABR USB Also Serves a Completely Different Audience

Dizziness and vertigo clinics (vertigo and balance clinics) are a buyer segment entirely different from pediatric audiology clinics. Here, the purchasing decision rests with ENT specialists focused on balance disorders, or with neurology clinics. Featuring VEMP clearly and separately on this page, rather than as a buried extra line, opens a whole second market for the eABR USB, separate from the hearing test market.

Why Choose the eABR USB for ABR and VEMP Testing?

Multiple, Flexible Test Stimuli

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The device supports Click, adjustable Tone-Pip, and CW-Chirp stimuli, with control over click polarity (positive, negative, alternating). This flexibility allows the examiner to choose the most suitable stimulus for each diagnostic case.

Automated Assistance Functions That Reduce Human Error

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Advanced functions that help ensure accurate and reliable testing:

  • Automatic monitoring of electrode impedance before the test begins
  • Automatic Gain Control (AGC)
  • Automatic artefact rejection to clean the recording of patient movement
  • Automatic stop function once sufficient recording quality is reached

High Recording Accuracy, Even in a Standard Clinic Environment

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A 2-channel analog-to-digital converter (ADC) with 24-bit resolution and a 48 kHz sampling rate, plus a common-mode rejection ratio (CMRR) above 130 dB at 50/60 Hz. In simple terms, it filters the true brain signal from surrounding electrical mains interference very effectively, without needing a fully electrically shielded room.

Fully Customizable Test Protocols

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Examiners can build their own freely defined test protocols (ready-made example: Threshold-BERA for estimating hearing threshold), with easy curve handling and automatic coupler detection.

Truly Portable, Not Just "Transportable"

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Weighing just 140 g without accessories, with power consumption under 5 W, it runs entirely from a USB 2.0 port (bus-powered) with no external power adapter. You can easily carry it between exam rooms or even between clinic branches, which is rarely possible with larger evoked potential systems.

Automatic PDF Reports and Free Lifetime Software Updates

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Automatic PDF report export after every test, plus free lifetime online software updates with no annual subscription fees for the software itself.

Why Choose the eABR USB for ABR and VEMP Testing

Complete Technical Specifications of the eABR USB BERA / ABR System

A. Supported Test Types

Test Type Details
Auditory Brainstem Response (BERA/ABR) Core test: objective hearing threshold estimation, the main area of use
Auditory Steady-State Response (ASSR) Supported within the auditory evoked potentials category
Cervical Vestibular Evoked Myogenic Potentials (c-VEMP) Optional module: assesses saccule function and the inferior vestibular nerve
Ocular Vestibular Evoked Myogenic Potentials (oVEMP) Optional module: assesses utricle function and the superior vestibular nerve

B. General Specifications

Specification Value
Air Conduction Headphones (AC-Phones) Radioear DD45 shielded / Radioear IP 30 Bera
Analog-to-Digital Converter (ADC) 2 channels, 24-bit resolution, 48 kHz sampling rate
Common-Mode Rejection (CMR) Greater than 130 dB at 50/60 Hz
Maximum Number of Sweeps Up to 10,000 sweeps
Interface & Power Supply USB 2.0, powered directly from the port with no external adapter (bus-powered)
Compatible Operating Systems Windows 10 and Windows 11
Dimensions 55 × 155 × 25 mm (about the size of a remote control)
Weight 140 g (without accessories)
Power Consumption Less than 5 W
Operating Environment 15 °C to 35 °C, humidity below 75%
Certified International Standards EN 60645-7:2010 / 93/42/EEC
Country of Manufacture Germany (Made in Germany)

C. Acoustic Test Stimuli

Specification Value
Supported Stimulus Types Click, adjustable Tone-Pip, Continuous Wave Chirp (CW-Chirp)
Click Polarity Positive / Negative / Alternating
Masking Masking noise

D. Automated Assistance Functions

Function What It Does for the Examiner
Automatic Electrode Impedance Control Instant alert when an electrode is poorly attached, before the test starts
Automatic Gain Control (AGC) Automatically adjusts input sensitivity according to signal quality
Automatic Artefact Rejection Automatically excludes recordings contaminated by patient movement
Automatic Stop Function Ends the test as soon as sufficient recording quality is reached, with no manual intervention
Automated Coupler Detection Automatically recognizes the type of transducer/coupler in use

E. Software & Reporting Features

Feature Details
Digital Conversion Resolution 24-bit conversion for high-quality recordings
Freely Definable Protocols Build custom protocols, with a ready-made example: Threshold-BERA for hearing threshold estimation
Curve Handling Easy-to-use interface for processing and reviewing response curves
Report Export Automatic PDF report export after every test
Software Updates Free lifetime online updates, with no annual subscription fees
Diagnostic System Integration Full integration with eDM (Diagnostic Manager) and a unified patient database shared with other BioMed Jena devices

eABR USB vs. Leading Global Evoked Potential Systems

Criteria eABR USB (BioMed Jena) Interacoustics Eclipse GSI Audera Pro Natus Celesta
Country of Origin Germany Denmark United States United States
ABR/BERA Testing Yes Yes Yes Yes
ASSR Testing Yes (listed within the evoked potentials category) Yes (full module) Yes (full module) Not explicitly listed as a standard module
VEMP Testing (c-/o-) Yes (optional) Yes Not announced as a standard module Yes
ECochG / Cortical Responses (LLR) Not available Yes (add-on modules) Yes (add-on modules) Cortical responses available
Built-in OAE Testing No (separate eOAE device from the same manufacturer) Yes (built-in module) Yes (built-in module) Not directly integrated
Device Type Truly portable, remote-control-sized (140 g) Modular PC-connected platform Comprehensive desktop clinical system PC-connected system within the Maestro ecosystem
Advanced Stimuli (Chirp) CW-Chirp Full CE-Chirp family CE-Chirp and CE-Chirp Octave Band Not detailed in available sources
Integration with a Unified Diagnostic System Yes: one database shared with eAUDIO, eTYMP and eOAE via eDM Integrates with OtoAccess/NOAH Proprietary GSI software Natus Maestro ecosystem
Price Positioning (estimated, based on product type) Lower initial investment: a focused device without built-in OAE/ECochG modules Higher investment: comprehensive modular platform Higher investment: comprehensive clinical system Higher investment: part of an integrated ecosystem

An Honest Summary of the Comparison

If your clinic or hospital needs a single, all-in-one platform that combines ABR, ASSR, OAE, ECochG and cortical responses in one device for a highly advanced diagnostic center, the three larger platforms (Eclipse, Audera Pro, Celesta) offer greater technical depth, but at a much higher investment.

But if your priority is a truly portable, focused device for routine ABR/BERA testing in newborns and children, with the option to add VEMP without needing all the extra modules, and with direct integration with the rest of the BioMed Jena range (eAUDIO, eTYMP and eOAE) through a single patient database, the eABR USB delivers strong practical value in a smaller footprint and at a lower investment.

ABR Testing in Adults: Objective Neurological and Retrocochlear Assessment

EEG

Analyzing Response Waves I, III and V: The Basis of the Neurological Test

The test works by analyzing the latency of the five standard response waves (clinical focus is on waves I, III and V) and comparing the timing difference between the two ears, known as the Interaural Latency Difference.

An abnormally delayed wave V, or a large difference between the two ears, is among the signs that lead doctors to suspect a problem along the auditory nerve pathway.

The eDM software supplied with the device displays this analysis directly in a ready-made report, showing wave I/III/V latencies in milliseconds for each ear and each sound intensity.

Conditions BERA/ABR Helps Evaluate in Adults

BERA / ABR
  • Retrocochlear hearing loss and tumors of the auditory nerve or brainstem (such as acoustic neuroma)
  • Multiple sclerosis (MS) as a supporting tool for assessing involvement of the auditory neural pathway
  • Head injuries and stroke to functionally assess brainstem integrity
  • Certain infections affecting the auditory neural pathway
  • Unexplained tinnitus, vertigo or difficulty understanding speech, even when conventional hearing tests such as the eAUDIO USB show normal results. This is a diagnostic gap that objective neurological testing is specifically suited to fill
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Additional Specialized Use: Intraoperative Neuromonitoring

ABR is also used for intraoperative neuromonitoring during surgeries near the auditory nerve or brainstem, to immediately alert the surgeon to any change in the response that may signal a risk to the nerve during the operation.

Scope note: Some clinical sources describe a highly specialized use of BERA in assessing brainstem function in coma patients, as part of brain death determination protocols in neurological intensive care units. This is a real use, but it is rare and limited to large hospitals with specialized neurology departments.

Who Should Use the eABR USB? Ideal Clinics and Specialties for ABR/BERA Testing

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Hospitals and pediatric clinics that want to offer the confirmatory stage of newborn hearing screening (after the initial OAE test)
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Specialized newborn hearing screening centers that need to cover the full two-stage protocol
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ENT (ear, nose and throat) departments for diagnosing asymmetric hearing loss or cases where behavioral audiometry is difficult
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Specialized dizziness, vertigo and balance clinics, using the optional VEMP module
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Cochlear implant centers as part of the comprehensive pre-surgical diagnostic assessment (alongside the eTYMP USB)
Who Should Use the eABR USB Ideal Clinics and Specialties for ABRBERA Testing

Where to Buy the eABR USB in the UAE: Why Choose iHear

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Exclusive authorized distributor of German BioMed Jena devices in the UAE.
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Direct technical support and hands-on training for your clinic team on the device and the eDM software.
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Regular maintenance and calibration to ensure consistently accurate clinical results.
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Documented spare parts and warranty through a single official distribution channel.
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Local office in Al Ain, UAE, close to our customers, not just remote support.
📍 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 Your Clinic May Need

Device Use How It Relates to the eABR USB
eOAE Otoacoustic emissions (OAE) testing, the first step in newborn hearing screening Used together in the complete newborn hearing screening pathway
eAUDIO USB 2-channel diagnostic audiometer For full behavioral assessment once the child is old enough to cooperate
eTYMP USB Middle ear analyzer (tympanometry + ESRT for cochlear implants) Completes cochlear implant assessment, neurally (eABR) and mechanically (eTYMP)

eABR USB FAQs: ABR / BERA Testing and VEMP Questions Answered

The eABR USB is a portable auditory brainstem response (ABR/BERA) system from the German manufacturer BioMed Jena. It records the activity of the auditory nerve and brainstem in response to sound and, with an optional module, also measures vestibular evoked myogenic potentials (VEMP) used to assess vertigo and balance disorders.
An auditory brainstem response (ABR) test, also called BERA (brainstem evoked response audiometry), is an objective hearing test. It records the tiny electrical signals produced by the auditory nerve and brainstem in response to sounds such as clicks or tone pips, using small electrodes on the skin. Because it does not depend on the patient's response, it is used to estimate hearing thresholds and to check the auditory nerve pathway in babies, children and adults.
In practice, yes. Both terms refer to the same electrical signal (the auditory brainstem response). BERA is the name commonly used in clinics when the test is used specifically to estimate hearing threshold, and it is the term most clinics and hospitals in the region use. You will find the two terms used interchangeably in most medical sources.
Small adhesive electrodes are placed on the forehead and behind the ears, and sounds are played through earphones while the system records the brain's electrical response. The patient lies still, and babies are usually tested during natural sleep. The test usually takes somewhere between 30 and 90 minutes, depending on the number of ears, stimuli and sound levels tested and on how settled the patient is.
No. The ABR test is non-invasive and painless. It uses adhesive electrodes on the skin and sounds played through earphones, with no needles. It is widely used with newborns and infants, who are usually tested while sleeping naturally.
Newborns and infants usually do not need sedation, as the test is performed during their natural sleep. Older children who struggle to stay calm may need light sedation, at the discretion of the treating doctor.
An ABR test can be performed at any age, from newborns to adults, because it does not rely on the patient's cooperation. It is especially useful for newborns, infants and young children, and for anyone who cannot give reliable behavioral responses to sound.
ABR results appear as a series of waves (I to V) within roughly the first 10 milliseconds after a sound. Clinically, waves I, III and V matter most: wave I mainly reflects the auditory nerve, wave III the lower brainstem, and wave V the upper brainstem pathway. A delayed wave V, or a large latency difference between the two ears, can lead clinicians to suspect a problem along the auditory pathway. The eDM software displays wave latencies and interpeak intervals (I-III, III-V, I-V) for each ear and sound level in a ready report.
Yes. ABR is widely used to estimate hearing threshold objectively by lowering the sound level step by step until wave V can no longer be identified. The eABR USB supports freely definable test profiles, with a Threshold-BERA profile given as an example in the manufacturer's datasheet.
A diagnostic ABR records the full response waveform at one or more sound levels, and a clinician interprets it to estimate thresholds and assess the neural pathway. Automated ABR (AABR) is a screening version that uses a fixed sound level and an algorithm to give a simple pass or refer result. The eABR USB is a diagnostic evoked potentials system with automatic assistance functions such as automatic artefact rejection and automatic stop. If you need dedicated AABR screening protocols, please confirm availability with iHear.
Because OAE tests only the cochlea and cannot detect auditory neuropathy spectrum disorder (ANSD), a condition where the first part of the ear works normally but the signal does not reach the brain properly. ABR testing, which the eABR USB performs, is the test able to detect this condition.
eAUDIO USB is a behavioral test that needs the patient's cooperation. eOAE tests the physical response of the cochlea only. eABR USB is a fully objective test that measures the actual neural pathway up to the brainstem and needs no conscious cooperation, so it works even while a baby sleeps.
Functionally, yes. The UAE Ministry of Health and Prevention (MOHAP) runs an early newborn hearing screening program that follows the internationally standard pathway: an OAE test first, then ABR for referred babies and high-risk cases (such as a long NICU stay). The eABR USB is designed to cover the ABR part of that pathway.
Yes. Its very small size (about the size of a remote control, 140 g) makes it practical to move between infant beds inside the unit.
Yes, through the optional VEMP module (cVEMP and oVEMP), used particularly in diagnosing superior semicircular canal dehiscence syndrome and as a supporting test when evaluating other conditions such as Meniere's disease.
cVEMP (cervical VEMP) is recorded from a neck muscle and mainly reflects the function of the saccule and the inferior vestibular nerve. oVEMP (ocular VEMP) is recorded from muscles around the eyes and mainly reflects the function of the utricle and the superior vestibular nerve. Together they give complementary information about the balance organs, and both are available on the eABR USB as an optional module.
No. Meniere's disease remains primarily a clinical diagnosis based on symptoms and a comprehensive evaluation. VEMP is used as a supporting tool that adds helpful information, not as a replacement for full clinical assessment.
Yes. With the optional cVEMP and oVEMP module, the device can be used solely to assess the vestibular system in dizziness and vertigo clinics, completely separate from hearing tests.
The eABR USB supports click, adjustable tone-pip and CW-Chirp stimuli. Click polarity can be set to positive, negative or alternating, and masking noise is available.
Up to 10,000 sweeps, with automatic gain control and artefact rejection to improve the quality of the recorded signal.
According to the manufacturer's datasheet: 2-channel 24-bit analog-to-digital converter at 48 kHz, common-mode rejection above 130 dB at 50/60 Hz, up to 10,000 sweeps, Radioear DD45 shielded or IP 30 Bera transducers, dimensions of 55 x 155 x 25 mm, weight of 140 g without accessories, power consumption below 5 W, Windows 10/11 software and automatic PDF export. Operating conditions are 15 to 35 °C and below 75% humidity.
According to the manufacturer's datasheet, the eABR USB conforms to EN 60645-7:2010 (the standard for auditory brainstem response measuring instruments) and 93/42/EEC (the medical devices directive). Contact the iHear team for the current certificates and documentation for your facility.
No. The device comes with free lifetime software updates, and the eDM software does not require a separate license for each workstation.
Both are European-standard systems for ABR and VEMP testing. The main practical difference is that the eABR USB comes as one very compact unit with an optional VEMP module built into the same device, and with eDM software that needs no per-workstation license, while the Eclipse relies on a base platform plus separately priced add-on modules.
The price varies depending on the configuration and the optional VEMP module. Contact the iHear team for a customized quote for your facility.
To confirm the registration status and the official documentation your facility requires, please contact the iHear team directly. They will provide all the necessary documents and certificates before purchase.
Yes. iHear provides full hands-on training on the device and the eDM software, plus regular maintenance, calibration and direct technical support.
In the UAE, the eABR USB is available through iHear, the authorized distributor of BioMed Jena devices, with offices in Abu Dhabi and Al Ain. iHear provides local technical support, training and maintenance. Contact the team by WhatsApp or phone to request a quote.
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