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customized FS-3224

by Qingdao Bestex Rubber & Plastic Products Co., Ltd. 2 variants

customized FS-3224 is a Class I device made by Qingdao Bestex Rubber & Plastic Products Co., Ltd., listed in FDA GUDID since 16 Jun 2023 (UDI-DI 06921340873113), 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 Number06921340873113 UDI-DI Date16 Jun 2023ListedStatusListed 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  • Withdrawn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
customized
Generic name
Face splash shield, single-use
Model / reference
FS-3224
Primary DI / UDI-DI
06921340873113
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

Similar devices

Other devices filed under FDA product code LYU (Accessory, Surgical Apparel).

Other devices from Qingdao Bestex Rubber & Plastic Products Co., Ltd.

See all devices from Qingdao Bestex Rubber & Plastic Products Co., Ltd. →

Properties

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