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Phonak Sky L90-SP

FDA UDI

Class II (US FDA UDI)

by Sonova AG

Identity

Trade Name
Phonak Sky L90-SP FDA UDI
Generic Name
Air-conduction hearing aid, behind-the-ear FDA UDI
Model / Reference
(precious pink) FDA UDI

Identifiers

Catalog Number
050-1115-T3 FDA UDI
Primary DI / UDI-DI
07613389665239 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 Sky L90-SP by Sonova AG — 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
Sonova AG

Sources (1)

  • FDA UDI 9fe73488-363c-4994-b06e-a1c120280b9b 33 fields · synced May 31, 2026