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Conmed QL6132

by Conmed Corporation

Ref QL6132

Conmed QL6132 is a device classified as Class IIa in the EU and Class I in the US made by Conmed Corporation, registered in EUDAMED on 7 Apr 2026 (Basic UDI-DI B-10845854036525) and listed in FDA GUDID since 14 Oct 2021 (UDI-DI 10845854036525), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10845854036525 Basic UDI-DI 10845854036525UDI-DIDate7 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854036525 UDI-DI Date14 Oct 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854036525 registered 7 Apr 2026 Active
  • FDA GUDID UDI-DI 10845854036525 listed 14 Oct 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854036525
  2. Registered EUDAMED B-10845854036525

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  • Withdrawn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, QuickLatch
Model / Ref / Catalog
QL6132
Primary DI / UDI-DI
10845854036525
Basic UDI-DI
B-10845854036525
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

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

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)