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Rectal tube

by Medirekt partner s.r.o. Czech Republic EUDAMED

Ref 574301 EMDN G020301

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859422418RECTALTUBEQJ Basic UDI-DIDate11 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Rectal tube
Model / Reference
574301
Primary DI / UDI-DI
08594224180140
Basic UDI-DI
859422418RECTALTUBEQJ
EMDN Code
G020301 Rectal tubes
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
CZ-MF-000053703

Other devices from Medirekt partner s.r.o.

See all devices from Medirekt partner s.r.o. →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED ff709989-5628-455b-ad75-de8641b0e515 61 fields · synced 23 Oct 2026