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A Plus 1

by A Plus International, Inc 259 variants

A Plus 1 (LS-0418-XS) is a Class I device made by A Plus International, Inc, listed in FDA GUDID since 19 Oct 2022 (UDI-DI 00683534840054), 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 Number00683534840054 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  • Withdrawn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
Radiopaque woven surgical sponge
Model / Ref / Catalog
1, LS-0418-XS
Description
Bulk Lap Sponges , 4"X18", X-Ray Detectable With String, Prewashed, Steam Pretreatment, White, No Optical Brightener, 5 Pc(s)/Bundle, 800 Pc(s)/Case
Primary DI / UDI-DI
00683534840054
FDA product code
NAB
GMDN term
Radiopaque woven surgical sponge
Device class
Class I
Regulation number
878.4014
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NAB (Gauze / Sponge,Nonresorbable For External Use).

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)