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Morton Medical

by Morton Medikal San ve Tic A.Ş. Türkiye EUDAMED

Ref MN 125-09

EMDN R03020101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-8698940541299JF Basic UDI-DIDate26 Apr 2022RegisteredStatusActive

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 24 Oct 2026

Device Name
Reusable Rebreatingbags Silicone
Model / Reference
MN 125-09
Primary DI / UDI-DI
D-8698940541299JF
Basic UDI-DI
B-8698940541299JF
EMDN Code
R03020101 Anaesthesia balloons
Device Class
Class IIa
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000020441

Other devices from Morton Medikal San ve Tic A.Ş.

See all devices from Morton Medikal San ve Tic A.Ş. →

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • 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 566765e7-297a-45b0-ab49-0b5b6d0ac6d6 61 fields · synced 24 Oct 2026