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No Brand 72205421

by Smith & Nephew, Inc.

No Brand 72205421 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 15 Jul 2020 (UDI-DI 00885556781579), 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 Number00885556781579 UDI-DI Date15 Jul 2020ListedStatusListed 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  • Withdrawn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
No Brand
Generic name
Face splash shield, single-use
Model / Ref / Catalog
72205421
Primary DI / UDI-DI
00885556781579
FDA product code
LYU
GMDN term
Face splash shield, single-use
Device class
Class I
Regulation number
878.4040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Face splash shield, single-use

Similar devices

Other devices filed under FDA product code LYU (ACCESSORY, SURGICAL APPAREL).

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)