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AIDA connect 20205501-140

by Karl Storz SE & CO. KG

AIDA connect 20205501-140 is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551356500), 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 Number04048551356500 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
AIDA connect
Generic name
Operating room audiovisual data/device management system
Model / reference
20205501-140
Primary DI / UDI-DI
04048551356500
FDA product code
LLZ
GMDN term
Operating room audiovisual data/device management system
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Operating room audiovisual data/device management system

Similar devices

Other devices filed under FDA product code LLZ (System, image processing, radiological).

Other devices from Karl Storz SE & CO. KG

See all devices from Karl Storz SE & CO. KG →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)