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eSuction ET2000

by Endo-Therapeutics Inc.

Ref ET2000

eSuction ET2000 is a Class I device made by Endo-Therapeutics Inc., registered in EUDAMED on 26 May 2026 (Basic UDI-DI B-00816207020969) and listed in FDA GUDID since 21 Sep 2022 (UDI-DI 00816207020969), active as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00816207020969 Basic UDI-DI 00816207020969UDI-DIDate26 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00816207020969 UDI-DI Date21 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00816207020969 registered 26 May 2026 Active
  • FDA GUDID UDI-DI 00816207020969 listed 21 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00816207020969
  2. Registered EUDAMED B-00816207020969

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  • Withdrawn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
eSuction
Generic name
Gastrointestinal/airway foreign body retrieval basket, single-use
Device name
Foreign Body Retrieval
Model / Ref / Catalog
ET2000
Primary DI / UDI-DI
00816207020969
Basic UDI-DI
B-00816207020969
FDA product code
FGX
EMDN code
G03050199 Digestive endoscopy, retrieval devices - other
GMDN term
Gastrointestinal/airway foreign body retrieval basket, single-use
Device class
Class I
Regulation number
876.4730
EU registration type
Legacy device (under a directive)
EU market of registration
Malta
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 19 Millimeter
Length — 230 Centimeter

Related devices

Category: Gastrointestinal/airway foreign body retrieval basket, single-use

Other devices from Endo-Therapeutics Inc.

See all devices from Endo-Therapeutics Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (16, all answered No)