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Aed W1616-45

by National Advanced Endoscopy Devices, Inc.

Aed W1616-45 is a Class I device made by National Advanced Endoscopy Devices, Inc., listed in FDA GUDID since 11 Aug 2017 (UDI-DI 00848657015783), 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 Number00848657015783 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  • Withdrawn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
Open-surgery ligation clip applier
Model / reference
W1616-45
Primary DI / UDI-DI
00848657015783
FDA product code
NWV
GMDN term
Open-surgery ligation clip applier
Device class
Class I
Regulation number
884.1720
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery ligation clip applier

Similar devices in this category

Other devices filed under Open-surgery ligation clip applier.

Other devices from National Advanced Endoscopy Devices, Inc.

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    Class II

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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)