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AMT G-JET® Winged Luer Adapter with Syringe E4-7000

by Applied Medical Technology, Inc. 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

1 closed

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 Number00842071136406 UDI-DI Date3 Oct 2025ListedStatusListed GUDID: in commercial distribution

Recalls

1 recall · FDA

    • Terminated Z-1497-2016 FDA Class II initiated 26 Jan 2016

    The firm received complaints that the product is shorter in length than indicated on the label.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
AMT G-JET® Winged Luer Adapter with Syringe
Generic Name
General-purpose syringe, single-use
Model / Ref / Catalog
E4-7000, 4-7000
Primary DI / UDI-DI
00842071136406
510(k) Number
FDA Product Code
KNT
GMDN Term
General-purpose syringe, single-use
Device Class
Class II
Regulation Number
876.5980
GUDID distribution status
In Commercial Distribution

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Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

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