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Halyard 32789

by Avanos Medical, Inc.

Halyard 32789 (RBW-5U) is a Class II device made by Avanos Medical, Inc., listed in FDA GUDID since 5 Sep 2016 (UDI-DI 10680651327892), 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 Number10680651327892 UDI-DI Date5 Sep 2016ListedStatusListed 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  • Withdrawn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
Halyard
Generic name
Nerve-locating system
Model / Ref / Catalog
32789, RBW-5U
Primary DI / UDI-DI
10680651327892
FDA product code
BXN
GMDN term
Nerve-locating system
Device class
Class II
Regulation number
868.2775
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code BXN (STIMULATOR, NERVE, BATTERY-POWERED).

Other devices from Avanos Medical, Inc.

See all devices from Avanos Medical, Inc. →

Properties

  • Lot / batch number
Other properties (14, all answered No)