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Summit 2570-10-000

by Depuy (Ireland)

Ref 2570-10-000

Summit 2570-10-000 (257010000) is a Class I device made by Depuy (Ireland), registered in EUDAMED on 4 Nov 2025 (Basic UDI-DI 0603295a000288C) and listed in FDA GUDID since 24 Sep 2018 (UDI-DI 10603295143659), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

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/MDR EUDAMED Number0603295a000288C Basic UDI-DI 10603295143659UDI-DIDate4 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10603295143659 UDI-DI Date24 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0603295a000288C registered 4 Nov 2025 Active
  • FDA GUDID UDI-DI 10603295143659 listed 24 Sep 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10603295143659
  2. Registered EUDAMED 0603295a000288C

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Summit
Generic name
Device sterilization/disinfection container, reusable
Device name
Sterilization Tray
Model / Ref / Catalog
2570-10-000, 257010000
Primary DI / UDI-DI
10603295143659
Basic UDI-DI
0603295a000288C
Direct marketing DI
10603295143659
FDA product code
FSM
EMDN code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
GMDN term
Device sterilization/disinfection container, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Device sterilization/disinfection container, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Depuy (Ireland)

See all devices from Depuy (Ireland) →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (22, all answered No)