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Medline NON25856

by Medline Industries, Inc.

Medline NON25856 is a dissection sponge (FDA Class I) made by Medline Industries, Inc., listed in FDA GUDID since 11 Jun 2022 (UDI-DI 10080196746002), 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 Number10080196746002 UDI-DI Date11 Jun 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  • Withdrawn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
Medline
Generic name
Dissection sponge
Model / Ref / Catalog
NON25856
Primary DI / UDI-DI
10080196746002
FDA product code
GDY, NAB
GMDN term
Dissection sponge
Device class
Class I
Regulation number
878.4450, 878.4014
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dissection sponge

Similar devices

Other devices filed under FDA product code GDY (Gauze/sponge, internal, x-ray detectable).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)