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Conmed Aes-50SL

by Conmed Corporation

Ref AES-50SL

Conmed Aes-50SL is a device classified as Class IIb in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 14 Apr 2026 (Basic UDI-DI B-10653405004974) and listed in FDA GUDID since 10 Nov 2017 (UDI-DI 10653405004974), 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-10653405004974 Basic UDI-DI 10653405004974UDI-DIDate14 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10653405004974 UDI-DI Date10 Nov 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10653405004974 registered 14 Apr 2026 Active
  • FDA GUDID UDI-DI 10653405004974 listed 10 Nov 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10653405004974
  2. Registered EUDAMED B-10653405004974

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  • Withdrawn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
Endoscopic electrosurgical handpiece/electrode, bipolar, single-use
Device name
Orthopedic, Active, Instrument, Electrosurgical, Bipolar, Ablator Probe
Model / Ref / Catalog
AES-50SL
Primary DI / UDI-DI
10653405004974
Basic UDI-DI
B-10653405004974
FDA product code
GEI
EMDN code
K02030101 Radiofrequency surgery electrodes, single-use
GMDN term
Endoscopic electrosurgical handpiece/electrode, bipolar, single-use
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.4400
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 IIb
GUDID
Class II

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

Related devices

Category: Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)