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XT Anesthesia Workstation (AWS) XT-AWS

by Omnicell, Inc.

XT Anesthesia Workstation (AWS) XT-AWS is a Class I device made by Omnicell, Inc., listed in FDA GUDID since 15 Feb 2021 (UDI-DI 00860006285012), 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 Number00860006285012 UDI-DI Date15 Feb 2021ListedStatusListed 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  • Withdrawn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
XT Anesthesia Workstation (AWS)
Generic name
Anaesthesia cabinet
Model / reference
XT-AWS
Primary DI / UDI-DI
00860006285012
FDA product code
BRY
GMDN term
Anaesthesia cabinet
Device class
Class I
Regulation number
868.6100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Anaesthesia cabinet

Similar devices

Other devices filed under FDA product code BRY (Cabinet, Table And Tray, Anesthesia).

Other devices from Omnicell, Inc.

See all devices from Omnicell, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)