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MediChoice 58158

by Owens & Minor Distribution, Inc.

MediChoice 58158 is a Class II device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 12 Mar 2025 (UDI-DI 20885632436045), 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 Number20885632436045 UDI-DI Date12 Mar 2025ListedStatusListed 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  • Withdrawn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
MediChoice
Generic name
Sterilization container filter, single-use
Model / reference
58158
Primary DI / UDI-DI
20885632436045
FDA product code
KCT
GMDN term
Sterilization container filter, single-use
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sterilization container filter, single-use

Other devices from Owens & Minor Distribution, Inc.

See all devices from Owens & Minor Distribution, Inc. →

Properties

  • Lot / batch number
Other properties (14, all answered No)