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BF890

by Steris Corporation

BF890 is a Class I device made by Steris Corporation, listed in FDA GUDID since 19 Jul 2023 (UDI-DI 00724995224240), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00724995224240 UDI-DI Date19 Jul 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  • Withdrawn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

Generic name
Universal operating table top
Model / Ref / Catalog
BF890
Description
CMAX X-Ray Vascular Accessory Package contains CF Radial Fistula Board and Catheter Extension. This package is used with the CMAX X-Ray Surgical Table.
Primary DI / UDI-DI
00724995224240
FDA product code
FQO
GMDN term
Universal operating table top
Device class
Class I
Regulation number
878.4960
GUDID distribution status
In Commercial Distribution

Related devices

Category: Universal operating table top

Similar devices in this category

Other devices filed under Universal operating table top.

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Over-the-counter
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)