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Standarddose rund, HDPE 500 ml, schwarzer Schraubdeckel mit PE-Dichteinlage, gefüllt mit Formaldehyd 4% phosphatgepuffert, Etikett mit Gefahrensymbolen aufgeklebt

by Engelbrecht Medizin- und Labortechnik GmbH

Ref S037670542

Active European Union

CE IVDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number426069618KAUK2 Basic UDI-DI 04260696181513UDI-DIDate19 Aug 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device Name
Standarddose rund, HDPE schwarzer Schraubdeckel mit PE-Dichteinlage, gefüllt mit Formaldehyd 4% phosphatgepuffert, Etikett mit Gefahrensymbolen aufgeklebt
Model / Reference
S037670542
Primary DI / UDI-DI
04260696181513
Basic UDI-DI
426069618KAUK2
Direct Marketing DI
04260696181513
EMDN Code
W05020103 Samples transport, bottles
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000053454

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Properties

Other properties (11)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No