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ReliOn 194346711994

by Walmart Stores

ReliOn 194346711994 is a Class II device made by Walmart Stores, listed in FDA GUDID since 20 May 2026 (UDI-DI 00194346711994), 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 Number00194346711994 UDI-DI Date20 May 2026ListedStatusListed 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  • Withdrawn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
ReliOn
Generic name
Autoinjector needle
Model / reference
194346711994
Description
100 Insulin Pen Needles 4mm x 32 Gauge (5/32" x 0.23mm)
Primary DI / UDI-DI
00194346711994
FDA product code
FMI
GMDN term
Autoinjector needle
Device class
Class II
Regulation number
880.5570
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FMI (Needle, Hypodermic, Single Lumen).

Other devices from Walmart Stores

See all devices from Walmart Stores →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)