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pezo

by Ulrich GmbH & Co. KG 3 variants

Ref CS 3315-07Model pezo-T

pezo (CS 3315-07) is a Class III device made by ulrich GmbH & Co. KG, registered in EUDAMED on 22 Jun 2026 (Basic UDI-DI 4052536000157QE) with CE/MDR certificate 20490GB450260605 valid until 23 Mar 2031, active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

23 Mar 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DNV MEDCERT GmbH

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4052536000157QE Basic UDI-DI 04052536228430UDI-DIDate22 Jun 2026RegisteredStatusActive

Official records

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 20490GB450260605 Active Supplemented

    Technical documentation EU MDR

    Certifier
    DNV MEDCERT GmbH 0482
    Issued
    5 Jun 2026
    Expires
    23 Mar 2031
    Reason
    Add device or group

Timeline

3 dated events

  1. Certificate issued EUDAMED 20490GB450260605
  2. Registered EUDAMED 4052536000157QE
  3. Certificate expires EUDAMED 20490GB450260605

Coverage

1 jurisdiction

Germany
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

  • Germany

Specification

EUDAMED

Model / reference
pezo-T, CS 3315-07
Primary DI / UDI-DI
04052536228430
Basic UDI-DI
4052536000157QE
EMDN code
P09070101 Spinal cages
Device class
Class III
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006411

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Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)