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Medical Action Industries E7500

by Medical Action Industries Inc.

Medical Action Industries E7500 is a dissection sponge (FDA Class I; FDA product code GDY, Gauze/Sponge, Internal, X-Ray Detectable) made by Medical Action Industries Inc., listed in FDA GUDID since 20 Aug 2016 (UDI-DI 10809160021996), 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 Number10809160021996 UDI-DI Date20 Aug 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  • Withdrawn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
Medical Action Industries
Generic name
Dissection sponge
Model / reference
E7500
Primary DI / UDI-DI
10809160021996
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

Other devices from Medical Action Industries Inc.

See all devices from Medical Action Industries Inc. →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)