Skip to content

A Plus 1

by A Plus International, Inc 38 variants

A Plus 1 (GS-4432-6S) is a device classified as Unclassified made by A Plus International, Inc, listed in FDA GUDID since 19 Oct 2022 (UDI-DI 00683534830123), 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 Number00683534830123 UDI-DI Date19 Oct 2022ListedStatusListed 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  • Withdrawn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
A Plus
Generic name
General-purpose surgical sponge
Model / Ref / Catalog
1, GS-4432-6S
Description
Bulk Gauze Sponges , 4"X4", 32 Ply, Steam Pretreated, Bleached White, Banded 10'S, 100 Pc(s)/Bag, 1000 Pc(s)/Case
Primary DI / UDI-DI
00683534830123
FDA product code
EFQ
GMDN term
General-purpose surgical sponge
Device class
U
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose surgical sponge

Similar devices

Other devices filed under FDA product code EFQ (Gauze/Sponge, Internal).

Other devices from A Plus International, Inc

See all devices from A Plus International, Inc →

Properties

  • Sterilise before use
  • Single use
  • Premarket exempt
Other properties (12, all answered No)