Skip to content

Aed 17-1719

by National Advanced Endoscopy Devices, 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00848657070683 UDI-DI Date25 Jun 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  • Withdrawn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
Aed
Generic name
Laparoscopic trocar blade, reusable
Model / reference
17-1719
Primary DI / UDI-DI
00848657070683
FDA product code
NWV
GMDN term
Laparoscopic trocar blade, reusable
Device class
Class I
Regulation number
884.1720
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from National Advanced Endoscopy Devices, Inc.

  • Aed AED2718B

    Class II

  • Aed AED2717B

    Class II

  • Aed AED2719B

    Class II

  • Aed 8815SB

    Class II

  • Aed 8810SB

    Class II

  • Aed 101012

    Class II

See all devices from National Advanced Endoscopy Devices, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number

Other properties (10)

  • Supplied sterile: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Expiration date: No
  • Manufacturing date: No