Skip to content

Percutaneous Tracheostomy Closed Suction System, 12 FR, 72 HRS

by R Vent Medi̇kal Üreti̇m A.Ş.

Ref 72121Model Closed Suction Systems, 72 Hrs, for Percutaneous Tracheostomy

Active European Union

CE MDD

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08681299502943 Basic UDI-DI 08681299502943UDI-DIDate17 Sep 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
Closed Suction Systems, 72 Hrs, for Percutaneous Tracheostomy, 72121
Primary DI / UDI-DI
08681299502943
Basic UDI-DI
B-08681299502943
EMDN Code
R050102 Closed-circuit respiratory suction and irrigation systems (non-endoscopic)
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000028282

Other devices from R Vent Medi̇kal Üreti̇m A.Ş.

See all devices from R Vent Medi̇kal Üreti̇m A.Ş. →

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