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Straight cup holder impactor positioner

by Keri Medical SA

Ref 112-A29300

Active European Union

CE MDR

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/MDR Number764018116018BD Basic UDI-DI 07640181162086UDI-DIDate29 Apr 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Impactors
Model / Reference
112-A29300
Primary DI / UDI-DI
07640181162086
Basic UDI-DI
764018116018BD
Direct Marketing DI
07640181162086
EMDN Code
L091104 Orthopaedic prostheses positioners, reusable
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000021960
Authorised representative
Keri Medical France FR-AR-000009590

Related devices

Category: Orthopaedic implant impactor, reusable

Other devices from Keri Medical SA

See all devices from Keri Medical SA →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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