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Nebulizer Set Newborn

by Tms Medi̇kal Plasti̇k Ürünleri̇ Sanayi̇ Ve Diş Ti̇caret Li̇mi̇ted Şi̇rketi̇

Ref T20161

Active European Union

CE MDR

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number869886383NEB3F Basic UDI-DI 86988638301280UDI-DIDate28 Nov 2024RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Nebulizer Set
Model / Reference
T20161
Primary DI / UDI-DI
86988638301280
Basic UDI-DI
869886383NEB3F
EMDN Code
R060101 Cold nebulisation systems
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000019237

Other devices from Tms Medi̇kal Plasti̇k Ürünleri̇ Sanayi̇ Ve Diş Ti̇caret Li̇mi̇ted Şi̇rketi̇

See all devices from Tms Medi̇kal Plasti̇k Ürünleri̇ Sanayi̇ Ve Diş Ti̇caret Li̇mi̇ted 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