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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
Hearing aid neck induction loop, wireless input FDA UDI
Device Name
Neckband Heairng Aid FDA UDI
Model / Reference
TL-651M FDA UDI
Description
Neckband Heairng Aid FDA UDI

Identifiers

Primary DI / UDI-DI
06937572805372 FDA UDI
FDA Product Code
QSM FDA UDI
GMDN Term
Hearing aid neck induction loop, wireless input FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Hearing aid neck induction loop, wireless input

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 Hearing aid neck induction loop, wireless input.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 33ae64b4-dd1f-4276-82e3-9db2f6cb00b5 33 fields · synced May 30, 2026