Skip to content

Bederní pás 100G, v.32cm, vel.4, bílá

by HANDICAP, a.s. EUDAMED

Active European Union

Ref 100G

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859404276018JQ Basic UDI-DIDate2 Sep 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  • Withdrawn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

Trade Name
Bederní pás 100G,v.32cm,vel.4,bílá
Bederní pás 100G,v.32cm,vel.2,bílá
Bederní pás 100G,v.32cm,vel.1,bílá
Bederní pás 100G,v.32cm,vel.6,bílá
Bederní pás 100G,v.32cm,vel.5,bílá
Bederní pás 100G,v.32cm,vel.7,bílá
Bederní pás 100G,v.32cm,vel.3,bílá
Device Name
Bederní pás 100G
Model / Reference
100G
Primary DI / UDI-DI
08594042761071, 08594042761057, 08594042761040, 08594042762955, 08594042761088, 08594042762962, 08594042761064
Basic UDI-DI
859404276018JQ
EMDN Code
Y060308 Lumbosacral spine orthoses
Device Class
Class I
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000001007

Other devices from HANDICAP, a.s.

See all devices from HANDICAP, a.s. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • 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