Skip to content

Snogg Aktiv

by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş 3 variants

Ref 4041

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868128511G10034R Basic UDI-DI 08681285122131UDI-DIDate18 May 2026RegisteredStatusActive

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  • Withdrawn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

Device Name
Aid Plaster
Model / Reference
4041
Primary DI / UDI-DI
08681285122131
Basic UDI-DI
868128511G10034R
EMDN Code
M0599 Medical plasters - other
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
TR-MF-000017199

Other devices from Honnes Sağlık ve Endüstriyel Ürünleri A.Ş

See all devices from Honnes Sağlık ve Endüstriyel Ürünleri A.Ş →

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