← Back to catalogue

Ha Hp 3 G4 Dbr

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 10951623Model BTE

by AS AUDIO-SERVICE GmbH

Identity

Trade Name
HA HP 3 G4 DBR EUDAMED
Audio Service FDA UDI
Generic Name
Air-conduction hearing aid, behind-the-ear FDA UDI
Device Name
Audio Service HA HP 3 G4 DBR Hearing Aid FDA UDI
Model / Reference
BTE EUDAMED
10951623 EUDAMED
HA HP 3 G4 DBR FDA UDI
Description
Audio Service HA HP 3 G4 DBR Hearing Aid FDA UDI

Identifiers

Catalog Number
10951623 FDA UDI
Primary DI / UDI-DI
04038953867681 EUDAMEDFDA UDI
Basic UDI-DI
B-04038953867681 EUDAMED
FDA Product Code
ESD FDA UDI
EMDN Code
Y2145060101 BEHIND-THE-EAR HEARING AIDS WITH RECEIVER IN THE DEVICE (BTE) EUDAMED
GMDN Term
Air-conduction hearing aid, behind-the-ear FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
874.3300 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Air-conduction hearing aid, behind-the-ear

Ha Hp 3 G4 Dbr by AS AUDIO-SERVICE GmbH — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Air-conduction hearing aid, behind-the-ear.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
DE-MF-000012295

Sources (2)

  • EUDAMED 4cb1b4e4-d683-49c1-b0f4-297f5362e9a2 61 fields · synced Oct 6, 2026
  • FDA UDI e4d58fa7-6391-466f-95c2-7a5885e9c816 36 fields · synced May 30, 2026