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Yankauer

by Conmed Corporation 8 variants

Ref 0038730, 0034980, 0034960, 9034980, 9034950, 0034950, 9034970

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

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

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10653405000631 Basic UDI-DI Date8 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10653405000631 UDI-DI Date5 Dec 2023ListedStatusListed GUDID: in commercial distribution

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

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use
Device Name
Non-orthopedic, Non-active, Instrument, Suction
Model / Ref / Catalog
0038730, 0034980, 0034960, 9034980, 9034950, 0034950, 9034970
Primary DI / UDI-DI
10653405000631, 10653405000341, 10653405000327, 40653405014929, 40653405014905, 10653405000310, 20653405014918
Basic UDI-DI
B-10653405000631, B-10653405000341, B-10653405000327, B-40653405014929, B-40653405014905, B-10653405000310, B-20653405014918
FDA Product Code
GCX
EMDN Code
A06010103 Cannulas and tips for aspiration and irrigation, single-use
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
880.6740
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide
Size
Length — 3 Meter
Length — 10 Feet

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterile YesEUDAMEDGUDIDNoEUDAMEDGUDID
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date NoGUDIDYesGUDID
  • Manufacturing Date YesGUDIDNoGUDID

Other properties (17)

  • Implantable: No
  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No