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BD Pyxis 1148-00

by CareFusion 303, Inc.

BD Pyxis 1148-00 is a Class I device made by CareFusion 303, Inc., listed in FDA GUDID since 29 Sep 2023 (UDI-DI 10885403517198), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885403517198 UDI-DI Date29 Sep 2023ListedStatusListed 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  • Withdrawn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
BD Pyxis
Generic name
Anaesthesia cabinet
Model / Ref / Catalog
1148-00
Primary DI / UDI-DI
10885403517198
FDA product code
BRY
GMDN term
Anaesthesia cabinet
Device class
Class I
Regulation number
868.6100
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Anaesthesia cabinet

Similar devices

Other devices filed under FDA product code BRY (CABINET, TABLE AND TRAY, ANESTHESIA).

Other devices from CareFusion 303, Inc.

See all devices from CareFusion 303, Inc. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)