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Starkey

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 63400-1Model Receiver-In-Canal (RIC)

by Starkey Laboratories Inc.

Identity

Trade Name
Starkey G Series AI 16 RIC R EUDAMED
STARKEY FDA UDI
Generic Name
Air-conduction hearing aid, receiver-in-canal FDA UDI
Device Name
G Series AI EUDAMED
Model / Reference
Receiver-In-Canal (RIC) EUDAMED
63400-1 EUDAMED
Starkey G Series AI 16 RIC R FDA UDI

Identifiers

Primary DI / UDI-DI
00840388209646 EUDAMEDFDA UDI
Basic UDI-DI
0842318163406V3 EUDAMED
FDA Product Code
KLW FDA UDI
OSM FDA UDI
EMDN Code
Y2145060102 BEHIND-THE-EAR HEARING AIDS WITH RECEIVER IN THE CANAL (RIC, RITE) EUDAMED
GMDN Term
Air-conduction hearing aid, receiver-in-canal FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
874.3400 FDA UDI
874.3305 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

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-canalTinnitus masking application software

Starkey by Starkey Laboratories Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Tinnitus masking application software.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI 8722a745-ddea-4c92-87e9-1f364606dd33 33 fields · synced Jul 26, 2026
  • EUDAMED ef55e822-bfc4-42d3-9770-d2be35257f0b 61 fields · synced Jul 26, 2026