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Agss

by Medicop - specialna oprema d.o.o.

Ref 3-en-Instruction_manual_AGSS_plant v1.4Model AGSS

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 Number3838578EQUSPEAGS788192P57 Basic UDI-DI 93838578000531UDI-DIDate12 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  • Withdrawn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
Anesthetic Gas Scavenging System
Model / Reference
AGSS, 3-en-Instruction_manual_AGSS_plant v1.4
Primary DI / UDI-DI
93838578000531
Basic UDI-DI
3838578EQUSPEAGS788192P57
Direct Marketing DI
93838578000531
EMDN Code
Z120309 Medical/medicinal gas pipeline systems and related accessories
Device Class
Class I
EU market of registration
Slovenia

Manufacturer details

EUDAMED SRN
SI-MF-000002144

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Properties

  • Administering Medicine

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
  • Measuring Function: No
  • Incorporates Medicinal Product: No