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Aed 32-4404

by National Advanced Endoscopy Devices, Inc.

Aed 32-4404 is a Class II device made by National Advanced Endoscopy Devices, Inc., listed in FDA GUDID since 11 Aug 2017 (UDI-DI 00848657020923), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00848657020923 UDI-DI Date11 Aug 2017ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
Urethrotome
Model / reference
32-4404
Primary DI / UDI-DI
00848657020923
FDA product code
EZO
GMDN term
Urethrotome
Device class
Class II
Regulation number
876.4770
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Urethrotome

Other devices from National Advanced Endoscopy Devices, Inc.

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    Class II

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    Class II

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    Class II

  • Aed 8815SB

    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, all answered No)