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Delta Xtend

by DePuy Ireland UC Ireland EUDAMED

Ref 1307-38-003Model DELTA XTEND Humeral PE Cup

EMDN P090104010202

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0603295a000878U Basic UDI-DIDate28 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 743997 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    13 Jul 2026
    Expires
    17 Jul 2028
    Reason
    Change approved

Specification

EUDAMED · synced 23 Oct 2026

Device Name
DELTA XTEND Humeral PE Cup
Model / Reference
DELTA XTEND Humeral PE Cup, 1307-38-003
Primary DI / UDI-DI
10603295272007
Basic UDI-DI
0603295a000878U
EMDN Code
P090104010202 Epiphysary humeral components for reverse prostheses - humeral cups
Device Class
Class III
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
IE-MF-000007377

Other devices from DePuy Ireland UC

See all devices from DePuy Ireland UC →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 10603295272007|0603295A000878U 61 fields · synced 23 Oct 2026