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Aed 120-301-350

by National Advanced Endoscopy Devices, Inc.

Aed 120-301-350 is a Class I device made by National Advanced Endoscopy Devices, Inc., listed in FDA GUDID since 10 Jul 2017 (UDI-DI 00848657017350), 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 Number00848657017350 UDI-DI Date10 Jul 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  • Withdrawn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 surgical procedure kit, non-medicated, reusable
Model / reference
120-301-350
Primary DI / UDI-DI
00848657017350
FDA product code
NBH
GMDN term
Arthroscopic surgical procedure kit, non-medicated, reusable
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 surgical procedure kit, non-medicated, reusable

Other devices from National Advanced Endoscopy Devices, Inc.

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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)