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DAS4031

by Fairmont Medical Products Pty Ltd Australia EUDAMED

Ref DAS40331Model DAS4031

EMDN A99

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-09330453300787 Basic UDI-DIDate16 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Arthroflush Set
Model / Reference
DAS4031, DAS40331
Primary DI / UDI-DI
09330453300787
Basic UDI-DI
B-09330453300787
EMDN Code
A99 Devices for administration, withdrawal and collection - other
Device Class
Class IIa
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
AU-MF-000005217
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Fairmont Medical Products Pty Ltd

See all devices from Fairmont Medical Products Pty Ltd →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (10)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED de0f8566-017b-4b91-9acd-5e7d5d600edd 61 fields · synced 22 Oct 2026