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Einweg-Sekretbehältersystem für Allegra M30

by ASSKEA GmbH

Ref 1510214HL21

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426058604SetNG Basic UDI-DI 04260586042030UDI-DIDate4 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  • Withdrawn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
Procedure Pack Accessories
Model / Reference
1510214HL21
Primary DI / UDI-DI
04260586042030
Basic UDI-DI
426058604SetNG
EMDN Code
A060399 Fluid collection bags and systems - other
Device Class
Class I
Medical Purpose
The sets consist of several accessories for the suction devices and consist of class 1 medical devices. The sets are necessary for the aspirators to perform their intended use.

Manufacturer details

EUDAMED SRN
DE-PR-000030721

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Properties

Other properties (1)

  • Sterile: No