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Accessory Tray ICV1230

by Corcym Inc.

Ref ICV1230Model Trays

Accessory Tray ICV1230 is a Class I device made by Corcym Inc., registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI 8022057ACCTRAYJ8) and listed in FDA GUDID since 1 Apr 2021 (UDI-DI 08022057014801), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number8022057ACCTRAYJ8 Basic UDI-DI 08022057014801UDI-DIDate29 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08022057014801 UDI-DI Date1 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 8022057ACCTRAYJ8 registered 29 Apr 2026 Active
  • FDA GUDID UDI-DI 08022057014801 listed 1 Apr 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08022057014801
  2. Registered EUDAMED 8022057ACCTRAYJ8

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  • Withdrawn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
Accessory Tray
Generic name
Instrument tray, reusable
Device name
Trays
Model / reference
ICV1230, Trays
Primary DI / UDI-DI
08022057014801
Basic UDI-DI
8022057ACCTRAYJ8
Direct marketing DI
08022057014801
FDA product code
DWS
EMDN code
L070799 Cardiac surgery instruments, reusable - other
GMDN term
Instrument tray, reusable
Device class
Class I
Regulation number
870.4500
EU registration type
Standard device
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under CARDIAC SURGERY INSTRUMENTS, REUSABLE.

Other devices from Corcym Inc.

  • TriMemo TRIM-26

    Class II
  • TriMemo TRIM-28

    Class II
  • TriMemo TRIM-30

    Class II
  • TriMemo TRIM-32

    Class II

See all devices from Corcym Inc. →

Properties

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