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Medline NON27600AG

by Medline Industries, Inc.

Medline NON27600AG is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 14 Oct 2016 (UDI-DI 10884389123867), 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 Number10884389123867 UDI-DI Date14 Oct 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  • Withdrawn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
Medline
Generic name
Eye splash shield, single-use
Model / Ref / Catalog
NON27600AG
Primary DI / UDI-DI
10884389123867
FDA product code
FXX
GMDN term
Eye splash shield, single-use
Device class
Class II
Regulation number
878.4040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Eye splash shield, single-use

Similar devices

Other devices filed under FDA product code FXX (Mask, surgical).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

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