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Henry Schein 1016279

by Henry Schein, Inc.

Ref 1016279Model TF-227 (HS)

Henry Schein 1016279 is a surgical soft-tissue manipulation forceps (EU MDD Class I; FDA Class I; FDA product code GEN, Forceps, General & Plastic Surgery) made by Henry Schein, Inc., registered in EUDAMED on 28 May 2026 (Basic UDI-DI B-00304040134740) and listed in FDA GUDID since 16 May 2019 (UDI-DI 00304040134740), 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-00304040134740 Basic UDI-DI 00304040134740UDI-DIDate28 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00304040134740 UDI-DI Date16 May 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00304040134740 registered 28 May 2026 Active
  • FDA GUDID UDI-DI 00304040134740 listed 16 May 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00304040134740
  2. Registered EUDAMED B-00304040134740

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  • Withdrawn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
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device name
Holding Instruments
Model / Ref / Catalog
1016279, TF-227 (HS)
Primary DI / UDI-DI
00304040134740 EUDAMED
00304040022757 GUDID
Basic UDI-DI
B-00304040134740
FDA product code
GEN
EMDN code
L031308 Surgical and anatomical tweezers, reusable
GMDN term
Surgical soft-tissue manipulation forceps, tweezers-like, 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
00304040134740
GUDID
00304040022757

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00304040134740; FDA GUDID lists 00304040022757), so their flags are not compared.

Related devices

Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Similar devices in this category

Other devices filed under SURGICAL AND ANATOMICAL TWEEZERS, 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)