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Bernafon

FDA UDI

Class II (US FDA UDI)

by Bernafon, Inc.

Identity

Trade Name
Bernafon FDA UDI
Generic Name
Air-conduction hearing aid, receiver-in-the-ear FDA UDI
Device Name
CT5 NR, PS MAC CANTEO 5 FDA UDI
Model / Reference
119361 FDA UDI
Description
CT5 NR, PS MAC CANTEO 5 FDA UDI

Identifiers

Primary DI / UDI-DI
05711584021491 FDA UDI
FDA Product Code
OSM FDA UDI
GMDN Term
Air-conduction hearing aid, receiver-in-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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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
MRI Safety
MR Unsafe FDA UDI

Category: Air-conduction hearing aid, receiver-in-the-ear

Bernafon by Bernafon, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bernafon, Inc.

Sources (1)

  • FDA UDI 5a966180-3d88-4e49-a501-fd141a8a93ec 34 fields · synced Jun 8, 2026