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Henry Schein 1029023

by Henry Schein, Inc.

Ref 1029023Model TF-211

Henry Schein 1029023 is a device classified as Class IIa in the EU and Class I in the US made by Henry Schein, Inc., registered in EUDAMED on 9 Jun 2026 (Basic UDI-DI B-10304040062125) and listed in FDA GUDID since 28 Dec 2020 (UDI-DI 10304040062125), 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-10304040062125 Basic UDI-DI 10304040062125UDI-DIDate9 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10304040062125 UDI-DI Date28 Dec 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10304040062125 registered 9 Jun 2026 Active
  • FDA GUDID UDI-DI 10304040062125 listed 28 Dec 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10304040062125
  2. Registered EUDAMED B-10304040062125

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  • Withdrawn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
Henry Schein
Generic name
Dental suction system
Device name
Surgical Aspirator Tips
Model / Ref / Catalog
1029023, TF-211
Primary DI / UDI-DI
10304040062125
Basic UDI-DI
B-10304040062125
FDA product code
EHZ
EMDN code
Q019001 Saliva aspirators and saliva absorbents
GMDN term
Dental suction system
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.6640
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 Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)