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Aicon JJ800

by Aesculap AG

Ref JJ800

Aicon JJ800 is a device classified as Class I in the EU and Class II in the US made by Aesculap AG, registered in EUDAMED on 21 Oct 2025 (Basic UDI-DI 403923900000113926) and listed in FDA GUDID since 28 Nov 2020 (UDI-DI 04046955279357), active as of 12 Nov 2026.

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

CE MDR

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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number403923900000113926 Basic UDI-DI 04046955279357UDI-DIDate21 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04046955279357 UDI-DI Date28 Nov 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 403923900000113926 registered 21 Oct 2025 Active
  • FDA GUDID UDI-DI 04046955279357 listed 28 Nov 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046955279357
  2. Registered EUDAMED 403923900000113926

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
AESCULAP Aicon® EUDAMED
Aicon GUDID
Generic name
Device sterilization/disinfection container, reusable
Model / Ref / Catalog
JJ800
Primary DI / UDI-DI
04046955279357
Basic UDI-DI
403923900000113926
Direct marketing DI
04046955279357
FDA product code
KCT
EMDN code
S010401 Trays, baskets, tubs for sterilisation and their components
GMDN term
Device sterilization/disinfection container, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6850
EU registration type
Standard device
EU market of registration
Germany
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 I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Device sterilization/disinfection container, reusable

Similar devices in this category

Other devices filed under TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS.

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

  • Sterilise before use
  • Over-the-counter
  • Lot / batch number
Other properties (22, all answered No)