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risa S

by audifon GmbH & Co. KG 9 variants

Ref 030239-9808-325-1720Model Hearing aid

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-030239-9808-325-1720VT Basic UDI-DI D-030239-9808-325-1720VTUDI-DIDate27 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD-030239-9808-325-1720VT UDI-DI Date21 Nov 2024ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
risa S EUDAMED
audifon GUDID
Generic Name
Air-conduction hearing aid, behind-the-ear
Model / Ref / Catalog
Hearing aid, 030239-9808-325-1720, risa S
Description
audifon risa S -- nougat BTE
Primary DI / UDI-DI
D-030239-9808-325-1720VT EUDAMED
EADF030239980832517201 GUDID
Basic UDI-DI
B-030239-9808-325-1720VT
FDA Product Code
OSM
EMDN Code
Y2145060101 Behind-the-ear hearing aids with receiver in the device (bte)
GMDN Term
Air-conduction hearing aid, behind-the-ear
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
874.3305
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Hearing aid
030239-9808-325-1720
GUDID
risa S
Primary DI / UDI-DIEUDAMED
D-030239-9808-325-1720VT
GUDID
EADF030239980832517201
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
DE-MF-000008355

Other devices from audifon GmbH & Co. KG

  • rega XS

    Class IIa
  • Power

    Class IIa
  • rega R

    Class IIa
  • He-S

    Class IIa
  • He-P

    Class IIa
  • offen

    Class IIa

See all devices from audifon GmbH & Co. KG →

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (19)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No