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Microflex Dgp-350-Xs

by Ansell Healthcare Product

Microflex Dgp-350-Xs is a Class I device made by Ansell Healthcare Product, listed in FDA GUDID since 14 Mar 2022 (UDI-DI 00769799140013), 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 Number00769799140013 UDI-DI Date14 Mar 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  • Withdrawn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
Microflex
Generic name
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial
Model / Ref / Catalog
DGP-350-XS
Primary DI / UDI-DI
00769799140013
FDA product code
LYY
GMDN term
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Other devices from Ansell Healthcare Product

See all devices from Ansell Healthcare Product →

Properties

  • Single use
  • Contains latex
  • Over-the-counter
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)