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Schraubdose 35 ml gefüllt mit Formaldehyd 4% phosphatgepuffert, Etikett mit Gefahrensymbolen aufgeklebt, in Schraubdose 100 ml mit Saugeinlage

by Engelbrecht Medizin- und Labortechnik GmbH 2 variants

Ref S084842.

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number426069618SANKU Basic UDI-DI 04260696180721UDI-DIDate2 Jun 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  • Withdrawn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
Schraubdose gefüllt mit Formaldehyd 4% phosphatgepuffert, Etikett mit Gefahrensymbolen aufgeklebt
Model / Reference
S084842.
Primary DI / UDI-DI
04260696180721
Basic UDI-DI
426069618SANKU
Direct Marketing DI
04260696180721
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