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EndoTExtractor ET2070

by Endo-Therapeutics, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816207021744 UDI-DI Date3 Mar 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
EndoTExtractor
Generic Name
Gastrointestinal/airway foreign body retrieval basket, single-use
Model / Ref / Catalog
ET2070
Primary DI / UDI-DI
00816207021744
FDA Product Code
PTS
GMDN Term
Gastrointestinal/airway foreign body retrieval basket, single-use
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution
Size
Length — 230 Centimeter
Outer Diameter — 2.6 Millimeter

Other devices from Endo-Therapeutics, Inc.

See all devices from Endo-Therapeutics, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No