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Tianle

FDA UDI

Class I (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-650F FDA UDI
Description
Neckband Heairng Aid FDA UDI

Identifiers

Primary DI / UDI-DI
06937572802449 FDA UDI
FDA Product Code
QUF FDA UDI
GMDN Term
Hearing aid neck induction loop, wireless input 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

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 I — 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 cb074adb-bc8c-4f57-a32a-009535c37bdb 33 fields · synced Jun 1, 2026