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SharpSafety 8781

by Cardinalhealth

SharpSafety 8781 is a Class II device made by Cardinalhealth, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10884521022171), 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 Number10884521022171 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
SharpSafety
Generic name
Sharps container
Model / Ref / Catalog
8781
Primary DI / UDI-DI
10884521022171
FDA product code
FMI
GMDN term
Sharps container
Device class
Class II
Regulation number
880.5570
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 8 Gallon

Similar devices

Other devices filed under FDA product code FMI (Needle, hypodermic, single lumen).

Other devices from Cardinalhealth

See all devices from Cardinalhealth →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
Other properties (12, all answered No)