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Phonak

FDA UDI

Class I (US FDA UDI)

by Phonak, Inc.

Identity

Trade Name
Phonak FDA UDI
Generic Name
Air-conduction hearing aid, receiver-in-canal FDA UDI
Device Name
Phonak Audéo Q90-10 (champagne) FDA UDI
Model / Reference
050-0079-P5 FDA UDI
Description
Phonak Audéo Q90-10 (champagne) FDA UDI

Identifiers

Catalog Number
050-0079-P5 FDA UDI
Primary DI / UDI-DI
07613275095072 FDA UDI
FDA Product Code
ESD FDA UDI
GMDN Term
Air-conduction hearing aid, receiver-in-canal 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Air-conduction hearing aid, receiver-in-canal

Phonak by Phonak, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Phonak, Inc.

Sources (1)

  • FDA UDI afb4a8c1-9557-4f0c-82f0-b3ae24340fa9 35 fields · synced Jun 6, 2026