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Aed 17-1790

by National Advanced Endoscopy Devices, Inc.

Aed 17-1790 is a Class I device made by National Advanced Endoscopy Devices, Inc., listed in FDA GUDID since 22 Nov 2017 (UDI-DI 00848657018739), 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 Number00848657018739 UDI-DI Date22 Nov 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  • Withdrawn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
Arthroscopic obturator
Model / reference
17-1790
Primary DI / UDI-DI
00848657018739
FDA product code
NBH
GMDN term
Arthroscopic obturator
Device class
Class I
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Arthroscopic obturator

Similar devices in this category

Other devices filed under Arthroscopic obturator.

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

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (10, all answered No)