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Henry Schein 1004018

by Henry Schein, Inc.

Ref 1004018Model TF-227 (HS)

Henry Schein 1004018 is a Class I device made by Henry Schein, Inc., registered in EUDAMED on 28 May 2026 (Basic UDI-DI B-00304040136317) and listed in FDA GUDID since 16 May 2019 (UDI-DI 00304040136317), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00304040136317 Basic UDI-DI 00304040136317UDI-DIDate28 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00304040136317 UDI-DI Date16 May 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00304040136317 registered 28 May 2026 Active
  • FDA GUDID UDI-DI 00304040136317 listed 16 May 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00304040136317
  2. Registered EUDAMED B-00304040136317

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  • Withdrawn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
General-purpose surgical scissors, reusable
Device name
Holding Instruments
Model / Ref / Catalog
1004018, TF-227 (HS)
Primary DI / UDI-DI
00304040136317 EUDAMED
00304040022535 GUDID
Basic UDI-DI
B-00304040136317
FDA product code
LRW
EMDN code
L010403 Surgical dissection scissors, reusable
GMDN term
General-purpose surgical scissors, reusable
Device class
Class I
Regulation number
878.4800
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
00304040136317
GUDID
00304040022535

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00304040136317; FDA GUDID lists 00304040022535), so their flags are not compared.

Related devices

Category: General-purpose surgical scissors, reusable

Similar devices in this category

Other devices filed under SURGICAL DISSECTION SCISSORS, REUSABLE.

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)