Skip to content

MOBILIS LumboIntense Back support, 26 cm, L

by Sigvaris Spółka Akcyjna EUDAMED

Active European Union

Ref 314511Model MOBILIS LumboIntense Pas lędźwiowy

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5906699LumboIntenseLJ Basic UDI-DIDate9 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
MOBILIS LumboIntense Pas lędźwiowy
Model / Reference
MOBILIS LumboIntense Pas lędźwiowy, 314511
Primary DI / UDI-DI
05906699002033
Basic UDI-DI
5906699LumboIntenseLJ
EMDN Code
Y060308 Lumbosacral spine orthoses
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000004824

Other devices from Sigvaris Spółka Akcyjna

See all devices from Sigvaris Spółka Akcyjna →

Properties

  • Contains Latex

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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