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ALM Tube + Nadelelektrode I.D. 7.5, O.D. 10.3

by inomed Medizintechnik GmbH

Ref 530946Model 530943

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 Number42503076IZS150CC Basic UDI-DI 14250307612021UDI-DIDate12 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  • Withdrawn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
ALM Tube + Nadelelektrode I.D. 6.0, O.D. 8.2
Model / Reference
530943, 530946
Primary DI / UDI-DI
14250307612021
Basic UDI-DI
42503076IZS150CC
EMDN Code
R01030201 Endotracheal tubes, cuffed, not reinforced
Device Class
Class IIa
Medical Purpose
The product is indicated for use in the operating room during surgeries that require oral intubation of the trachea for anaesthesia, ventilation management and EMG-monitoring of the nerve supplying the laryngeal musculature.

Manufacturer details

EUDAMED SRN
DE-PR-000019534

Related devices

Category: Basic endotracheal tube, single-use

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Properties

  • Sterile