Skip to content

SurgiTrackSM 450070F844

by Owens & Minor Distribution, Inc.

SurgiTrackSM 450070F844 is a Class II device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 28 Oct 2026 (UDI-DI 10885632542213), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885632542213 UDI-DI Date28 Oct 2026ListedStatusListed 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  • Withdrawn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
SurgiTrackSM
Generic name
General surgical procedure kit, non-medicated, single-use
Model / reference
450070F844
Primary DI / UDI-DI
10885632542213
FDA product code
LRO
GMDN term
General surgical procedure kit, non-medicated, single-use
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Other devices from Owens & Minor Distribution, Inc.

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

Properties

  • Single use
  • Contains latex
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)