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Akas Infusions

by Akas Medical Equipment 5 variants

Ref SYRU4004Model AKAS SYRU 4004

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-INMF00002906340042T Basic UDI-DI D-INMF00002906340042TUDI-DIDate2 Mar 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Syringe Infusion Pump
Model / Reference
AKAS SYRU 4004, SYRU4004
Primary DI / UDI-DI
D-INMF00002906340042T
Basic UDI-DI
B-INMF00002906340042T
EMDN Code
Z12030301 Infusion pumps
Device Class
Class IIb
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
IN-MF-000029063
Authorised representative
Amstermed B.V. NL-AR-000001971

Other devices from Akas Medical Equipment

Properties

  • Administering Medicine

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No