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Beamer QED-6001

by Qed, Inc.

Beamer QED-6001 is a Class II device made by Qed, Inc., listed in FDA GUDID since 21 May 2025 (UDI-DI 00860013851507), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860013851507 UDI-DI Date21 May 2025ListedStatusListed 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  • Withdrawn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
Beamer
Generic name
General-purpose light source
Model / reference
QED-6001
Primary DI / UDI-DI
00860013851507
FDA product code
FTD
GMDN term
General-purpose light source
Device class
Class II
Regulation number
878.4580
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose light source

Similar devices

Other devices filed under FDA product code FTD (Lamp, Surgical).

Other devices from Qed, Inc.

See all devices from Qed, Inc. →

Properties

  • Premarket exempt
Other properties (14, all answered No)