Skip to content

Nasal Specula KILLIAN X = 35 mm

by Durable Hospital Supplies

Ref 18-233-35

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 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G198Speculum59 Basic UDI-DI +G19818233350EUDI-DIDate26 Mar 2024RegisteredStatusActive

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  • Withdrawn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
Speculum, vaginal, Sims, retractor, double-ended, large
Model / Reference
18-233-35
Primary DI / UDI-DI
+G19818233350E
Basic UDI-DI
++G198Speculum59
EMDN Code
L149004 ENT speculums, reusable
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
PK-MF-000025646
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Durable Hospital Supplies

See all devices from Durable Hospital Supplies →

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