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Tianle

FDA UDI

Class II (US FDA UDI)

by Zhongshan Tianle Hearing Technology Co., Ltd.

Identity

Trade Name
TIANLE FDA UDI
Generic Name
Air-conduction hearing aid, canal FDA UDI
Device Name
In The Canal Hearing Aid FDA UDI
Model / Reference
TW-812G FDA UDI
Description
In The Canal Hearing Aid FDA UDI

Identifiers

Primary DI / UDI-DI
06937572803613 FDA UDI
FDA Product Code
QUG FDA UDI
GMDN Term
Air-conduction hearing aid, canal FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3305 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Air-conduction hearing aid, canal

Tianle by Zhongshan Tianle Hearing Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Air-conduction hearing aid, canal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de3a86f8-ad32-47c7-bfd2-4fc1aadcabf5 33 fields · synced May 29, 2026