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Bederní pás zdvojený tah 100B, vel.3, černá

by HANDICAP, a.s. EUDAMED

Active European Union

Ref 100B

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859404276031JG Basic UDI-DIDate17 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  • Withdrawn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 zdvojený tah 100B,vel.3,černá
Bederní pás zdvojený tah 100B,vel.1,černá
Bederní pás zdvojený tah 100B,vel.5,černá
Bederní pás zdvojený tah 100B,vel.4,černá
Device Name
Bederní pás 100B
Model / Reference
100B
Primary DI / UDI-DI
08594042760869, 08594042760845, 08594042760883, 08594042760876
Basic UDI-DI
859404276031JG
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