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V. Mueller 23275-440

by Steris Corporation

V. Mueller 23275-440 (23275440) is a dissection sponge (FDA Class I; FDA product code GDI, Dissector, Surgical, General & Plastic Surgery) made by Steris Corporation, listed in FDA GUDID since 12 Jul 2018 (UDI-DI 70885403067633), 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 Number70885403067633 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  • Withdrawn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
23275-440, 23275440
Primary DI / UDI-DI
70885403067633
FDA product code
GDI
GMDN term
Dissection sponge
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dissection sponge

Similar devices

Other devices filed under FDA product code GDI (DISSECTOR, SURGICAL, GENERAL & PLASTIC SURGERY).

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)