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NA Table Extension

by Steris Corporation GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00724995363352 UDI-DIDate8 Oct 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Generic Name
Patient transfer sliding board
Model / Ref / Catalog
Table Extension, BF00514
Primary DI / UDI-DI
00724995363352
FDA Product Code
BWN
GMDN Term
Patient transfer sliding board
Device Class
Class I
Regulation Number
878.4950
GUDID distribution status
In Commercial Distribution

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Premarket Exempt
  • Manufacturing Date

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No