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Persona Medical

FDA UDI

Class II (US FDA UDI)

by Persona Medical

Identity

Trade Name
Persona Medical FDA UDI
Generic Name
Air-conduction hearing aid, behind-the-ear FDA UDI
Device Name
Hearing Device incorporating advanced algorithms and simple controls for volume & memory settings for different environments. FDA UDI
Model / Reference
RxEars RX9 FDA UDI
Description
Hearing Device incorporating advanced algorithms and simple controls for volume & memory settings for different environments. FDA UDI

Identifiers

Primary DI / UDI-DI
00851362008179 FDA UDI
FDA Product Code
OSM FDA UDI
GMDN Term
Air-conduction hearing aid, behind-the-ear 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

Yes

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

Yes

FDA UDI

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

Persona Medical by Persona Medical — Class II — 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 95814dcc-80f5-4cd2-aa71-a6a21b86dc3d 33 fields · synced Jun 8, 2026