Tinearity Adapters

Primary DI
07350136210051
Brand
Tinearity Adapters
Company
Duearity AB
Model
G1
Catalog number
6042
Published
2023-07-28
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
KLWMasker, Tinnitus

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KLWMasker, TinnitusEar, Nose, Throat2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K223694000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K223694000Tinearity G1 (6103); Tinearity G1 Adapters x3 (6042)Duearity AB2023-06-30KLW

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07350136210020PrimaryGS10
07350136210051Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07350136210020073501362100207350136210020
07350136210051073501362100517350136210051

GMDN Terms#

Term, Definition table
TermDefinition
Bone-conduction tinnitus maskerA battery-powered acoustic device designed to provide ultrasonic broadband noise and/or sweep-frequency stimuli noise of sufficient intensity and bandwidth to mask tinnitus (a ringing sound in the ear or internal head noises) by neutralizing a patient’s perception of the symptoms for temporary relief. It consists of an out-of-ear miniature generator/amplifier with a piezoelectric element which conducts the noise to the inner ear across the skin and via the mastoid bone; it may be contained in a case worn behind-the-ear (BTE), attached to a headband, or hand-held by the user against the skin over the mastoid bone.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
353427191
Device count
3
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07350136210020Tinearity AdaptersG160422023-07-28
07350136210099TinearityG161032023-07-28
07350136210075TinearityG161032023-07-28

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
07613275596821PhonakSonova AGKLW2018-02-28
07613275596838PhonakSonova AGKLW2018-02-28
07613275596852PhonakSonova AGKLW2018-02-28
07613275596876PhonakSonova AGKLW2018-02-28
07613275596890PhonakSonova AGKLW2018-02-28
07613275596906PhonakSonova AGKLW2018-02-28
07613275596913PhonakSonova AGKLW2018-02-28
07613275596920PhonakSonova AGKLW2018-02-28
07613275596937PhonakSonova AGKLW2018-02-28
07613275596975PhonakSonova AGKLW2018-02-28
07613275597026PhonakSonova AGKLW2018-02-28
07613275601310PhonakSonova AGKLW2018-02-28
07613275601334PhonakSonova AGKLW2018-02-28
07613275601341PhonakSonova AGKLW2018-02-28
07613275601358PhonakSonova AGKLW2018-02-28
07613275601365PhonakSonova AGKLW2018-02-28
07613275601372PhonakSonova AGKLW2018-02-28
07613275601389PhonakSonova AGKLW2018-02-28
07613275601396PhonakSonova AGKLW2018-02-28
07613275601419PhonakSonova AGKLW2018-02-28
07613275601433PhonakSonova AGKLW2018-02-28
07613275601440PhonakSonova AGKLW2018-02-28
07613275601457PhonakSonova AGKLW2018-02-28
07613275601464PhonakSonova AGKLW2018-02-28
07613275601471PhonakSonova AGKLW2018-02-28
07613275601488PhonakSonova AGKLW2018-02-28
07613275601495PhonakSonova AGKLW2018-02-28
07613275601525PhonakSonova AGKLW2018-02-28
07613275601532PhonakSonova AGKLW2018-02-28
07613275601549PhonakSonova AGKLW2018-02-28