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Conmed UQL6111

by Conmed Corporation

Ref UQL6111

Conmed UQL6111 is a device classified as Class IIa in the EU and Class I in the US made by Conmed Corporation, registered in EUDAMED on 3 Apr 2026 (Basic UDI-DI B-10845854605899) and listed in FDA GUDID since 12 Oct 2023 (UDI-DI 10845854605899), active as of 23 Oct 2026.

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

CE MDD

Valid until

No date given

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

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10845854605899 Basic UDI-DI 10845854605899UDI-DIDate3 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854605899 UDI-DI Date12 Oct 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854605899 registered 3 Apr 2026 Active
  • FDA GUDID UDI-DI 10845854605899 listed 12 Oct 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854605899
  2. Registered EUDAMED B-10845854605899

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  • Withdrawn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

Trade name
Conmed
Generic name
Endoscope sheath, reusable
Device name
Orthopedic, Non-active, Instrument, Sheath/Bridge, UQL QuickLatch
Model / Ref / Catalog
UQL6111
Primary DI / UDI-DI
10845854605899
Basic UDI-DI
B-10845854605899
FDA product code
NBH
EMDN code
L1907 Arthroscopic surgery cannulas, reusable
GMDN term
Endoscope sheath, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.1100
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Endoscope sheath, reusable

Similar devices in this category

Other devices filed under ARTHROSCOPIC SURGERY CANNULAS, REUSABLE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)