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Pubistrap H21

by Groupe Sober SAS EUDAMED

Active European Union

Ref PUBISTRAP H21Model CEINTURE SOUTIEN LOMBAIRE H21

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03760035441342 Basic UDI-DIDate23 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Model / Reference
CEINTURE SOUTIEN LOMBAIRE H21, PUBISTRAP H21
Primary DI / UDI-DI
03760035441342
Basic UDI-DI
B-03760035441342
EMDN Code
Y060309 Thoracolumbosacral spine orthoses
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000017818

Other devices from Groupe Sober SAS

See all devices from Groupe Sober SAS →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No