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Demel wire guide Fig.2, 29cm/11½"

by IAA Surgical Instruments Company

Ref 26-182-02

Active European Union

CE MDR

Valid until

14 Jun 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++B832REPROBESDILATORSD8 Basic UDI-DIDate19 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Surgical Probes, Dilators & Sounds
Model / Reference
26-182-02
Primary DI / UDI-DI
+B832261820200
Basic UDI-DI
++B832REPROBESDILATORSD8
Direct Marketing DI
+B832261820200
EMDN Code
L0922 Orthopaedic surgery guides, reusable
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
PK-MF-000023042
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Iaa Surgical Instruments Co

See all devices from Iaa Surgical Instruments Co →

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