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Tomore

FDA UDI

Class I (US FDA UDI)

by Tomore Healthcare (Dongguan) Co., Ltd.

Identity

Trade Name
TOMORE FDA UDI
Generic Name
Air-conduction hearing aid acoustic tube FDA UDI
Device Name
Hearing Aid FDA UDI
Model / Reference
3308A FDA UDI
Description
Hearing Aid FDA UDI

Identifiers

Primary DI / UDI-DI
06977275990210 FDA UDI
FDA Product Code
QUF FDA UDI
GMDN Term
Air-conduction hearing aid acoustic tube FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Air-conduction hearing aid acoustic tube

A comprehensive hearing aid device designed for individuals with mild to moderate hearing loss. The TOMORE is a small, detachable device that conducts sound waves from an air-conduction hearing aid to an earmould, providing clear and effective audio.

Similar devices

Also classified as Air-conduction hearing aid acoustic tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d6eca1a3-f4c2-41e9-a3d6-9c0aab476cfc 33 fields · synced Oct 7, 2026