Skip to content

Henry Schein 1043375

by Henry Schein, Inc.

Ref 1043375Model TF-227 (HS)

Henry Schein 1043375 is a rubber dam punch (EU MDD Class I; FDA Class I; FDA product code EIE, Dam, Rubber) made by Henry Schein, Inc., registered in EUDAMED on 28 May 2026 (Basic UDI-DI B-00304040135969) and listed in FDA GUDID since 3 Jan 2020 (UDI-DI 00304040135969), 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-00304040135969 Basic UDI-DI 00304040135969UDI-DIDate28 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00304040135969 UDI-DI Date3 Jan 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00304040135969 registered 28 May 2026 Active
  • FDA GUDID UDI-DI 00304040135969 listed 3 Jan 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00304040135969
  2. Registered EUDAMED B-00304040135969

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  • Withdrawn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
Hsm EUDAMED
Henry Schein GUDID
Generic name
Rubber dam punch
Device name
Holding Instruments
Model / Ref / Catalog
1043375, TF-227 (HS)
Primary DI / UDI-DI
00304040135969 EUDAMED
00304040120279 GUDID
Basic UDI-DI
B-00304040135969
FDA product code
EIE
EMDN code
L031399 General surgery forceps, reusable - other
GMDN term
Rubber dam punch
Device class
Class I
Regulation number
872.6300
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 · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00304040135969
GUDID
00304040120279

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00304040135969; FDA GUDID lists 00304040120279), so their flags are not compared.

Related devices

Category: Rubber dam punch

Similar devices in this category

Other devices filed under GENERAL SURGERY FORCEPS, REUSABLE.

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)