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LIVIO Edge AI RIC 312

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 63192Model Livio Standard RIC

by Starkey Laboratories Inc.

Identity

Trade Name
LIVIO Edge AI RIC 312 EUDAMED
STARKEY FDA UDI
Generic Name
Air-conduction hearing aid, receiver-in-canal FDA UDI
Device Name
Livio Standard RIC EUDAMED
Model / Reference
Livio Standard RIC EUDAMED
63192 EUDAMED
STARKEY LIVIO EDGE AI 2400 RIC 312 FDA UDI

Identifiers

Catalog Number
63192-1, 63192-7, 63205-1 FDA UDI
Primary DI / UDI-DI
00842318179357 EUDAMEDFDA UDI
Basic UDI-DI
0842318163112UF EUDAMED
Direct Marketing DI
00842318179357 EUDAMED
FDA Product Code
OSM FDA UDI
KLW 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
874.3305 FDA UDI
874.3400 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-canal

LIVIO Edge AI RIC 312 by Starkey Laboratories Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000014382
Authorised Representative
Starkey Laboratories (Germany) GmbH DE-AR-000010831

Sources (2)

  • EUDAMED b2e8699a-eff8-4222-a739-715ef8c5f2e5 61 fields · synced Jul 14, 2026
  • FDA UDI 1f2739e3-a95b-4ff5-ba0d-ad1179123379 34 fields · synced May 30, 2026