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Microflex N485

by Ansell Healthcare Product

Microflex N485 is a Class I device made by Ansell Healthcare Product, listed in FDA GUDID since 14 Mar 2022 (UDI-DI 00683438144852), 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 Number00683438144852 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  • Withdrawn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
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / Ref / Catalog
N485
Primary DI / UDI-DI
00683438144852
FDA product code
LZA, LZC
GMDN term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Other devices from Ansell Healthcare Product

See all devices from Ansell Healthcare Product →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)