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Vitom 20916025AGA

by Karl Storz SE & CO. KG

Vitom 20916025AGA is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 21 Oct 2017 (UDI-DI 04048551347188), 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 Number04048551347188 UDI-DI Date21 Oct 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  • Withdrawn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
Vitom
Generic name
Surgical microscope video camera, sterilizable
Model / reference
20916025AGA
Primary DI / UDI-DI
04048551347188
FDA product code
OWN
GMDN term
Surgical microscope video camera, sterilizable
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical microscope video camera, sterilizable

Similar devices

Other devices filed under FDA product code OWN (Confocal optical imaging).

Other devices from Karl Storz SE & CO. KG

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

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
Other properties (12, all answered No)