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LT evo 25 – 50 kg 50 – 90 kg > 90 kg

by VBM Medizintechnik GmbH

Ref 32-10-209-1

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42501056-1.2.10-sy-RT Basic UDI-DI 04250105630220UDI-DIDate6 May 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Laryngeal Tubes - LT evo system
Model / Reference
32-10-209-1
Primary DI / UDI-DI
04250105630220
Basic UDI-DI
42501056-1.2.10-sy-RT
EMDN Code
R010202 Laryngeal tubes
Device Class
Class IIa
Medical Purpose
Supragiottic airway to temporarily secure the airway.

Manufacturer details

EUDAMED SRN
DE-PR-000019561

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Properties

  • Sterile