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RXEars

FDA UDI

Class I (US FDA UDI)

by Persona Medical

Identity

Trade Name
RXEars FDA UDI
Generic Name
Air-conduction hearing aid, behind-the-ear FDA UDI
Device Name
Hearing Device incorporating an adjustable rocker volume control and memory control to fit mild to moderate HL. May also be programmed at the factory for small variations. FDA UDI
Model / Reference
RX4 FDA UDI
Description
Hearing Device incorporating an adjustable rocker volume control and memory control to fit mild to moderate HL. May also be programmed at the factory for small variations. FDA UDI

Identifiers

Primary DI / UDI-DI
00851362008438 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

RXEars by Persona Medical — 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

Manufacturer
Persona Medical

Sources (1)

  • FDA UDI 21c2066b-b32b-4df5-8cea-a15ee156865b 33 fields · synced May 30, 2026