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pezo

by Ulrich GmbH & Co. KG EUDAMED

Active European Union

Ref CS 3331-08Model pezo-A

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4052536000155QA Basic UDI-DIDate22 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 20490GB450260605 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 0482
    Issued
    5 Jun 2026
    Expires
    23 Mar 2031
    Reason
    Add device or group

Specification

EUDAMED

Model / Reference
pezo-A, CS 3331-08
Primary DI / UDI-DI
04052536228683
Basic UDI-DI
4052536000155QA
EMDN Code
P09070101 Spinal cages
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006411

Other devices from ulrich GmbH & Co. KG

See all devices from ulrich GmbH & Co. KG →

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