Skip to content

Kurtarma Yeleği̇ (Ked Yeleği̇)

by Ems Mobi̇l Si̇stemler Anoni̇m Şi̇rketi̇ EUDAMED

Active European Union

Ref ET 370Model KURTARMA YELEĞİ

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8697606ET-M8 Basic UDI-DIDate9 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Ked Yeleği̇
Model / Reference
KURTARMA YELEĞİ, ET 370
Primary DI / UDI-DI
08697606581594
Basic UDI-DI
8697606ET-M8
Direct Marketing DI
08697606581594
EMDN Code
V080302 Patient positioning medical cushions
Device Class
Class I
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000033584

Other devices from Ems Mobi̇l Si̇stemler Anoni̇m Şi̇rketi̇

See all devices from Ems Mobi̇l Si̇stemler Anoni̇m Şi̇rketi̇ →

Properties

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