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Medline MDS73512

by Medline Industries, Inc.

Medline MDS73512 is a dissection sponge (FDA Class I; FDA product code GDY, Gauze/Sponge, Internal, X-Ray Detectable) made by Medline Industries, Inc., listed in FDA GUDID since 22 Mar 2021 (UDI-DI 10888277338906), 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 Number10888277338906 UDI-DI Date22 Mar 2021ListedStatusListed 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  • Withdrawn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
MDS73512
Primary DI / UDI-DI
10888277338906
FDA product code
GDY
GMDN term
Dissection sponge
Device class
Class I
Regulation number
878.4450
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)