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Hand Control

by Steris Corporation 8 variants

Hand Control (BF318) is a Class I device made by Steris Corporation, listed in FDA GUDID since 2 Apr 2021 (UDI-DI 00724995156909), 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 Number00724995156909 UDI-DI Date2 Apr 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  • Withdrawn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

Generic name
Operating room equipment remote control
Model / Ref / Catalog
Hand Control, BF318
Primary DI / UDI-DI
00724995156909
FDA product code
FQO
GMDN term
Operating room equipment remote control
Device class
Class I
Regulation number
878.4960
GUDID distribution status
In Commercial Distribution

Related devices

Category: Operating room equipment remote control

Similar devices in this category

Other devices filed under Operating room equipment remote control.

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)