Skip to content

V. Mueller 23275-680

by Steris Corporation

V. Mueller 23275-680 (23275680) is a dissection sponge (FDA Class I; FDA product code GDY, Gauze/Sponge, Internal, X-Ray Detectable) made by Steris Corporation, listed in FDA GUDID since 12 Jul 2018 (UDI-DI 70885403067770), 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 Number70885403067770 UDI-DI Date12 Jul 2018ListedStatusListed 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  • Withdrawn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
V. Mueller
Generic name
Dissection sponge
Model / Ref / Catalog
23275-680, 23275680
Primary DI / UDI-DI
70885403067770
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 Steris Corporation

See all devices from Steris Corporation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)