Soniton

GUDID 05714464150502

SONITON Z1.20 FW 1.0.0

Sbo Hearing A/S

Hearing aid wireless-fitting computer-aided set
Primary Device ID05714464150502
NIH Device Record Key9807b56d-02d3-4533-9f03-7d2d3b88206b
Commercial Distribution StatusIn Commercial Distribution
Brand NameSoniton
Version Model Number277532
Company DUNS306018410
Company NameSbo Hearing A/S
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com
Phone+4523648485
Emailsucc@demant.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105714464150502 [Primary]

FDA Product Code

KLWMasker, tinnitus

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-02-18
Device Publish Date2025-02-10

On-Brand Devices [Soniton]

05714464006601PERSONAL 3.3 FW 1.0.0
05714464006595PERSONAL 2.3 FW 1.0.0
05714464006588PERSONAL 1.3 FW 1.0.0
05714464150519SONITON Z1.10 FW 1.0.0
05714464150502SONITON Z1.20 FW 1.0.0

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