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Conmed Aes-30

by Conmed Corporation

Ref AES-30

Conmed Aes-30 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-30653405064149) and listed in FDA GUDID since 14 Oct 2020 (UDI-DI 30653405064149), 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-30653405064149 Basic UDI-DI 30653405064149UDI-DIDate14 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number30653405064149 UDI-DI Date14 Oct 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-30653405064149 registered 14 Apr 2026 Active
  • FDA GUDID UDI-DI 30653405064149 listed 14 Oct 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 30653405064149
  2. Registered EUDAMED B-30653405064149

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  • Withdrawn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-30
Primary DI / UDI-DI
30653405064149
Basic UDI-DI
B-30653405064149
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
Sterilisation method
Ethylene Oxide
Size
Angle — 30 degree
Length — 8.5 Centimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II
Sterilise before useEUDAMED
No
GUDID
Yes

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 30653405064149: EUDAMED states No, FDA GUDID states Yes.

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

Similar devices in this category

Other devices filed under RADIOFREQUENCY SURGERY ELECTRODES, SINGLE-USE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)