Unique device identifiers (GUDID)

Moxi S9-RX · (sand)

Sonova AG

DI 07613389840605In Commercial DistributionOSM
Open FDA's page for this record
Has donation ID number
false
Mri safety
MR Unsafe
Record status
Published
Is labeled as nrl
false
Is rx
false
Commercial distribution status
In Commercial Distribution
Public device record key
518a6199-4070-4bb1-b9fb-5767eef7fa84
Has serial number
true
Public version date
2026-08-03
Is direct marking exempt
true
Public version number
1
Labeler duns number
480662550
Is labeled as no nrl
false
Is single use
false
Is otc
false
Version or model number
(sand)
Has manufacturing date
true
Brand name
Moxi S9-RX
Is combination product
false
Is kit
false
Device count in base package
1
Is pm exempt
true
Has lot or batch number
false
Catalog number
050-6927-R8
Company name
Sonova AG
Public version status
New
Has expiration date
false
Is hct p
false
Publish date
2026-07-26
Sterilization
Is sterile
false
Is sterilization prior use
false
Identifiers
  1. ID
    07613389840605
    Type
    Primary
    Issuing agency
    GS1
Product codes
  1. Code
    OSM
    Name
    Hearing aid, air conduction with wireless technology
    Harmonized identifiers (openFDA)
    Device name
    Hearing Aid, Air-Conduction With Wireless Technology, Prescription
    Medical specialty description
    Ear, Nose, Throat
    Regulation number
    874.3305
    Device class
    2
  2. Code
    KLW
    Name
    Masker, Tinnitus
    Harmonized identifiers (openFDA)
    Device name
    Masker, Tinnitus
    Medical specialty description
    Ear, Nose, Throat
    Regulation number
    874.3400
    Device class
    2
Customer contacts
  1. Phone
    +41589280101
    Email
    info@sonova.com
Gmdn terms
  1. Code
    47169
    Name
    Air-conduction hearing aid, receiver-in-canal
    Implantable
    false
    Code status
    Active
    Definition

    A battery-powered acoustic device intended to compensate for impaired hearing by transmitting amplified sound waves to the eardrum through air. It consists of a microphone and an amplifier in a case behind-the-ear (BTE) connected, via a wire, to a receiver (speaker) in the ear canal [receiver-in-canal (RIC)]. The microphone receives sound waves and converts them into electrical signals which are increased by the amplifier and sent as sound waves, by the speaker, to the eardrum. The device is used for mild to profound hearing loss; most types are programmable to enable computerized adjustments for a patient's hearing loss and related factors.

Wholesale access for licensed clinicians.

Free to join: your NPI is checked against the federal registry at signup, then wholesale pricing and the professional shelves open.

Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.