← Back to catalogue

Phonak

FDA UDI

Class II (US FDA UDI)

by Phonak, Inc.

Identity

Trade Name
Phonak FDA UDI
Generic Name
Air-conduction hearing aid, behind-the-ear FDA UDI
Device Name
Phonak Naída Q30-UP (amber beige) FDA UDI
Model / Reference
050-0147-P2 FDA UDI
Description
Phonak Naída Q30-UP (amber beige) FDA UDI

Identifiers

Catalog Number
050-0147-P2 FDA UDI
Primary DI / UDI-DI
07613275148938 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

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, behind-the-ear

Phonak Naída Q30-UP, a high-performance behind-the-ear (BTE) hearing aid designed to compensate for mild to profound hearing loss. With its advanced air-conduction technology and wireless connectivity, this device provides clear sound and improved speech understanding.

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Phonak, Inc.

Sources (1)

  • FDA UDI 6dadba8f-5c3c-4ac6-9679-e651eb9192a9 35 fields · synced Jul 24, 2026