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4350F

by Smith & Nephew, Inc.

4350F is a Class II device made by Smith & Nephew, Inc., listed in FDA GUDID since 22 Oct 2015 (UDI-DI 00885556606902), 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 Number00885556606902 UDI-DI Date22 Oct 2015ListedStatusListed 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  • Withdrawn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
Surgical/orthopaedic lavage control unit
Model / Ref / Catalog
4350F
Primary DI / UDI-DI
00885556606902
FDA product code
HRX
GMDN term
Surgical/orthopaedic lavage control unit
Device class
Class II
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HRX (ARTHROSCOPE).

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)