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Nuear

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 63407-4Model Receiver-In-Canal (RIC)

by Starkey Laboratories Inc.

Identity

Trade Name
NuEar NE Series AI 12 RIC 312 EUDAMED
NUEAR 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
63407-4 EUDAMED
NuEar NE Series AI 12 RIC 312 FDA UDI

Identifiers

Primary DI / UDI-DI
00840388209530 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

Nuear 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

Manufacturer
Starkey Laboratories Inc.

Sources (2)

  • FDA UDI 4b0f80d7-17e1-4c6d-a0ce-2f8ed3f7be35 33 fields · synced Jun 19, 2026
  • EUDAMED 3c209e18-4483-43a8-a4a5-f7cad9160a2e 61 fields · synced Jun 19, 2026