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Suction canister

by Serres Oy

Ref 57348

Active European Union

CE MDR

Valid until

24 Oct 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS FIMKO OY

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 NumberFI22/00000016 Date24 Oct 2025IssuedStatusActive expires 24 Oct 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • FI22/00000016 Active Reissued

    Quality management system EU MDR

    Certifier
    SGS FIMKO OY 0598
    Issued
    24 Oct 2025
    Expires
    24 Oct 2030
    Valid from
    25 Oct 2025

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Suction canisters
Model / Reference
57348
Primary DI / UDI-DI
06418685063496
Basic UDI-DI
6418685SBS27S
Direct Marketing DI
06418685063496
EMDN Code
A06030401 Intraoperative suction containers
Device Class
Class I
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000004504

Other devices from Serres Oy

See all devices from Serres Oy →

Properties

  • Measuring Function

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
  • Administering Medicine: No
  • Incorporates Medicinal Product: No