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Ohrstöpsel Typ IA Gelb, 10 mm

by Merz Medizintechnik GmbH

Ref 71500079Model 75999999, 73000020

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426058541426058541165346 Basic UDI-DI 04260585411295UDI-DIDate19 Sep 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Trade Name
Ohrstöpsel Typ IA Gelb, 10 mm
MERZ Ohrstöpsel Typ IA Gelb 10 mm
Device Name
Ohrstöpsel
MERZ Ohrstöpsel Typ KR Gelb 3 mm
Model / Reference
75999999, 71500079, 73000020
Primary DI / UDI-DI
04260585411295
Basic UDI-DI
426058541426058541165346, 426058541MERZOhrstopselAF
Direct Marketing DI
04260585411295
EMDN Code
A03040204 Ear irrigation kits, single-use
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000010619

Other devices from Merz Medizintechnik GmbH

See all devices from Merz Medizintechnik GmbH →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No