Skip to content

LogiTube Lux Kit

by Surgical Innovations Ltd.

Ref LUXLIGHTKIT

LogiTube Lux Kit (LUXLIGHTKIT) is a Class I device made by Surgical Innovations Ltd., registered in EUDAMED on 27 Feb 2025 (Basic UDI-DI 5051986SISUG4H), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5051986SISUG4H Basic UDI-DI 05051986013640UDI-DIDate27 Feb 2025RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
LogiTube Gastric Calibration Tube
Model / reference
LUXLIGHTKIT
Primary DI / UDI-DI
05051986013640
Basic UDI-DI
5051986SISUG4H
EMDN code
Z12020402 Light sources for endoscopy and minimally invasive surgery
Device class
Class I
EU registration type
Standard device
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000012187
Authorised representative
CS Life Sciences Europe Ltd IE-AR-000004113

Related devices

Category: Endoscopic light source unit, line-powered

Similar devices in this category

Other devices filed under LIGHT SOURCES FOR ENDOSCOPY AND MINIMALLY INVASIVE SURGERY.

Other devices from Surgical Innovations Ltd.

See all devices from Surgical Innovations Ltd. →

Properties

Other properties (14, all answered No)