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ampli-mini R 2 L PH

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 050-1091-P167Model Sonova RIC hearing aids

by Sonova AG

Identity

Trade Name
ampli-mini R 2 L PH (sand beige) EUDAMED
ampli-mini R 2 L PH FDA UDI
Generic Name
Air-conduction hearing aid, receiver-in-canal FDA UDI
Device Name
Sonova RIC hearing aids EUDAMED
Model / Reference
Sonova RIC hearing aids EUDAMED
050-1091-P167 EUDAMED
(sand beige) FDA UDI

Identifiers

Catalog Number
050-1091-P167 FDA UDI
Primary DI / UDI-DI
07613389722482 EUDAMEDFDA UDI
Basic UDI-DI
07613389RICWJ 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

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, receiver-in-canal

ampli-mini R 2 L PH by Sonova AG — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sonova AG

Sources (2)

  • FDA UDI 5488089c-627a-4c47-9671-1d4947e0941e 33 fields · synced Jun 19, 2026
  • EUDAMED f7d29b7a-180f-4679-8704-433051db8491 61 fields · synced Jun 19, 2026