Skip to content

Neb-NSET4-83AP

by OMRON Healthcare Co., Ltd.

Ref NEB-NSET4-83AP

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number497547949725QB Basic UDI-DI 04975479497254UDI-DIDate6 Jul 2026RegisteredStatusActive EUDAMED: not on the EU market

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

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Neb-NSET4-83AP
Model / Reference
NEB-NSET4-83AP
Primary DI / UDI-DI
04975479497254
Basic UDI-DI
497547949725QB
EMDN Code
R03010304 Aerosol therapy kits
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
JP-MF-000007213
Authorised representative
OMRON Healthcare Europe B.V. NL-AR-000002683

Other devices from OMRON Healthcare Co., Ltd.

See all devices from OMRON Healthcare Co., Ltd. →

Properties

  • Administering Medicine

Other properties (12)

  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No