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DYNACUP standard HXLPE insert for 28 mm head Ø 46 AT

by Corin Ltd

Ref HLM812Model DynaCup Acetabular cup

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05056139206450 Basic UDI-DI 05056139206450UDI-DIDate17 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
DynaCup polyethylene inserts for use in total hip arthroplasty
Model / Reference
DynaCup Acetabular cup, HLM812
Primary DI / UDI-DI
05056139206450
Basic UDI-DI
B-05056139206450
EMDN Code
P090803040101 Standard polyethylene hip prostheses inserts
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
GB-MF-000008942
Authorised representative
CORIN FRANCE SAS FR-AR-000001192

Other devices from Corin Limited

See all devices from Corin Limited →

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