Skip to content

Encore 2018675

by Ansell Healthcare Product

Encore 2018675 is a Class I device made by Ansell Healthcare Product, listed in FDA GUDID since 26 Jan 2022 (UDI-DI 00884792208642), 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 Number00884792208642 UDI-DI Date26 Jan 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  • Withdrawn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
Encore
Generic name
Hevea-latex surgical glove, non-powdered, non-antimicrobial
Model / Ref / Catalog
2018675
Primary DI / UDI-DI
00884792208642
FDA product code
KGO
GMDN term
Hevea-latex surgical glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
878.4460
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hevea-latex surgical glove, non-powdered, non-antimicrobial

Other devices from Ansell Healthcare Product

See all devices from Ansell Healthcare Product →

Properties

  • Supplied sterile
  • Single use
  • Contains latex
  • Over-the-counter
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)