Skip to content

Aed 32-4216BW

by National Advanced Endoscopy Devices, Inc.

Aed 32-4216BW is a Class II device made by National Advanced Endoscopy Devices, Inc., listed in FDA GUDID since 7 May 2019 (UDI-DI 00848657087063), 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 Number00848657087063 UDI-DI Date7 May 2019ListedStatusListed 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  • Withdrawn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
Resectoscope
Model / reference
32-4216BW
Primary DI / UDI-DI
00848657087063
FDA product code
FDC
GMDN term
Resectoscope
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Resectoscope

Similar devices

Other devices filed under FDA product code FDC (RESECTOSCOPE, WORKING ELEMENT).

Other devices from National Advanced Endoscopy Devices, Inc.

  • Aed AED2718B

    Class II

  • Aed AED2717B

    Class II

  • Aed AED2719B

    Class II

  • Aed 8815SB

    Class II

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

Properties

  • Prescription use
  • Lot / batch number
  • Serial number
Other properties (12, all answered No)