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LITUS Xi- Peripheral Balloon Expandable Stent System

by Q3 Medical Germany GmbH 19 variants

Ref 13 QBX 090575F, 08 QBX 090365F, 08 QBX 080365F, 08 QBX 100175F, 08 QBX 070265F, 13 QBX 080175F, 08 QBX 050575F, 13 QBX 080265F, 08 QBX 100365F, 13 QBX 050575F, 13 QBX 050175F, 13 QBX 070265F, 08 QBX 090175F, 13 QBX 090175F, 08 QBX 100575F, 08 QBX 060265F, 13 QBX 100175F, 08 QBX 060365F, 13 QBX 070365F, 08 QBX 050265F, 13 QBX 070175F, 08 QBX 090265F, 08 QBX 050365F, 08 QBX 050175F, 13 QBX 090265F, 13 QBX 100365F, 13 QBX 080575F, 13 QBX 080365F

Active European Union

CE MDD

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04051649221703 Basic UDI-DI Date1 Nov 2023RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
13 QBX 090575F, 08 QBX 090365F, 08 QBX 080365F, 08 QBX 100175F, 08 QBX 070265F, 13 QBX 080175F, 08 QBX 050575F, 13 QBX 080265F, 08 QBX 100365F, 13 QBX 050575F, 13 QBX 050175F, 13 QBX 070265F, 08 QBX 090175F, 13 QBX 090175F, 08 QBX 100575F, 08 QBX 060265F, 13 QBX 100175F, 08 QBX 060365F, 13 QBX 070365F, 08 QBX 050265F, 13 QBX 070175F, 08 QBX 090265F, 08 QBX 050365F, 08 QBX 050175F, 13 QBX 090265F, 13 QBX 100365F, 13 QBX 080575F, 13 QBX 080365F
Primary DI / UDI-DI
04051649221703, 04051649221932, 04051649221895, 04051649221956, 04051649221840, 04051649221635, 04051649221789, 04051649221642, 04051649221970, 04051649221543, 04051649221512, 04051649221604, 04051649221918, 04051649221673, 04051649221987, 04051649221802, 04051649221710, 04051649221819, 04051649221611, 04051649221765, 04051649221598, 04051649221925, 04051649221772, 04051649221758, 04051649221680, 04051649221734, 04051649221666, 04051649221659
Basic UDI-DI
B-04051649221703, B-04051649221932, B-04051649221895, B-04051649221956, B-04051649221840, B-04051649221635, B-04051649221789, B-04051649221642, B-04051649221970, B-04051649221543, B-04051649221512, B-04051649221604, B-04051649221918, B-04051649221673, B-04051649221987, B-04051649221802, B-04051649221710, B-04051649221819, B-04051649221611, B-04051649221765, B-04051649221598, B-04051649221925, B-04051649221772, B-04051649221758, B-04051649221680, B-04051649221734, B-04051649221666, B-04051649221659
EMDN Code
P070402020102 Non-stainless steel peripheral vascular bare metal stents
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000008095

Other devices from Q3 Medical Germany GmbH

See all devices from Q3 Medical Germany GmbH →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • 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