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Clik

FDA UDI

Class I (US FDA UDI)

by Ear Technology Corporation

Identity

Trade Name
Clik FDA UDI
Generic Name
Air-conduction hearing aid, behind-the-ear FDA UDI
Device Name
air conduction hearing aid FDA UDI
Model / Reference
Clik FDA UDI
Description
air conduction hearing aid FDA UDI

Identifiers

Primary DI / UDI-DI
00810323002540 FDA UDI
FDA Product Code
ESD FDA UDI
GMDN Term
Air-conduction hearing aid, behind-the-ear 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Air-conduction hearing aid, behind-the-ear

Clik by Ear Technology Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Air-conduction hearing aid, behind-the-ear.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 42834d9c-d4b1-4220-8aae-2f741f6a3e65 33 fields · synced Jun 9, 2026