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PST Corp. 4700A

by Tray Plastic Sterilizing Corporation Inc

Ref 4700A

PST Corp. 4700A is a Class I device made by Tray Plastic Sterilizing Corporation Inc, registered in EUDAMED on 9 May 2026 (Basic UDI-DI 00810051834700AYM) and listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00810051830361), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number00810051834700AYM Basic UDI-DI 00810051830361UDI-DIDate9 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00810051830361 UDI-DI Date8 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 00810051834700AYM registered 9 May 2026 Active
  • FDA GUDID UDI-DI 00810051830361 listed 8 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00810051830361
  2. Registered EUDAMED 00810051834700AYM

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  • Withdrawn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
PST Corp.
Generic name
Instrument tray, reusable
Model / Ref / Catalog
4700A
Primary DI / UDI-DI
00810051830361
Basic UDI-DI
00810051834700AYM
Direct marketing DI
00810051830361
FDA product code
FSM
EMDN code
S010401 Trays, baskets, tubs for sterilisation and their components
GMDN term
Instrument tray, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS.

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Properties

  • Over-the-counter
  • Premarket exempt
Other properties (23, all answered No)