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Non-DEHP Microbore Epidural Yellow Striped Tubing Admin Set, Vented Vial Spike W/Vented 0.2 μm Filter, NRFit

by Zevex Inc.

Ref 380-4194Model 380-4192

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 linked in EUDAMED

A group certificate may exist

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 Number081484400816915DD Basic UDI-DI 10814844001485UDI-DIDate4 Aug 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Non-DEHP Epidural, Yellow Striped Tubing Admin Set, Non-Vent Spike, Vented 0.2 μm Filter, NRFit
Model / Reference
380-4192, 380-4194
Primary DI / UDI-DI
10814844001485
Basic UDI-DI
081484400816915DD
EMDN Code
Z12030385 Infusion instruments - consumables
Device Class
Class IIa
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
US-MF-000005937
Authorised representative
UAB Moog Vilnius LT-AR-000017784

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Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • 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