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EMG Endotracheal Tube

by Tianjin Plastics Research Institute Co., Ltd. EUDAMED

Active European Union

Ref 06944803631464

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6944803600120000GE Basic UDI-DIDate27 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • CN25/00007713 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 1639
    Issued
    30 Apr 2026
    Expires
    13 Nov 2030
    Reason
    Add device or group

Specification

EUDAMED

Device Name
EMG Endotracheal Tube
Model / Reference
06944803631464
Primary DI / UDI-DI
06944803631464
Basic UDI-DI
6944803600120000GE
EMDN Code
R01038001 Endotracheal tube cuffs inflation systems
Device Class
Class IIa
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000031209
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Tianjin Plastics Research Institute Co., Ltd.

See all devices from Tianjin Plastics Research Institute Co., Ltd. →

Properties

Show properties
  • Sterile
Other properties (12)
  • 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