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Maintenance Kit AIL0239

by Zyris, Inc.

Ref AIL0239

Maintenance Kit AIL0239 is a device classified as Class IIa in the EU and Class I in the US made by Zyris, Inc., registered in EUDAMED on 17 Aug 2026 (Basic UDI-DI B-00810032660628) and listed in FDA GUDID since 8 Apr 2024 (UDI-DI 00810032660628), 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-00810032660628 Basic UDI-DI 00810032660628UDI-DIDate17 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00810032660628 UDI-DI Date8 Apr 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00810032660628 registered 17 Aug 2026 Active
  • FDA GUDID UDI-DI 00810032660628 listed 8 Apr 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00810032660628
  2. Registered EUDAMED B-00810032660628

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  • Withdrawn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
Maintenance Kit
Generic name
Dental suction system
Model / Ref / Catalog
AIL0239
Primary DI / UDI-DI
00810032660628
Basic UDI-DI
B-00810032660628
FDA product code
EAZ
EMDN code
Q019001 Saliva aspirators and saliva absorbents
GMDN term
Dental suction system
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.4630
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
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: Dental suction system

Similar devices in this category

Other devices filed under SALIVA ASPIRATORS AND SALIVA ABSORBENTS.

Other devices from Zyris, Inc.

See all devices from Zyris, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)