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Henry Schein 1002407

by Henry Schein, Inc.

Ref 1002407Model TF-010

Henry Schein 1002407 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 29 May 2026 (Basic UDI-DI B-10304040073343) and listed in FDA GUDID since 17 Dec 2019 (UDI-DI 10304040073343), 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-10304040073343 Basic UDI-DI 10304040073343UDI-DIDate29 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10304040073343 UDI-DI Date17 Dec 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10304040073343 registered 29 May 2026 Active
  • FDA GUDID UDI-DI 10304040073343 listed 17 Dec 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10304040073343
  2. Registered EUDAMED B-10304040073343

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  • Withdrawn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
Carbide dental bur, reusable
Device name
Steel & TC Burs
Model / Ref / Catalog
1002407, TF-010
Description
Carbide Bur RA 37
Primary DI / UDI-DI
10304040073343 EUDAMED
00304040073346 GUDID
Basic UDI-DI
B-10304040073343
FDA product code
EJL
EMDN code
Z12110102 Dental drills
GMDN term
Carbide dental bur, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.3240
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
10304040073343
GUDID
00304040073346
Device classEUDAMED
Class IIa
GUDID
Class I

The registries describe this device under different primary UDI-DIs (EUDAMED lists 10304040073343; FDA GUDID lists 00304040073346), so their flags are not compared. 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: Carbide dental bur, reusable

Similar devices in this category

Other devices filed under INSTRUMENTS FOR DENTAL TREATMENT UNITS.

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)