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ORLocate Towel

by Steris Corporation 7 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10724995220966 UDI-DI Date7 Dec 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ORLocate
Generic Name
Radiopaque woven surgical sponge
Model / Ref / Catalog
ORLocate Towel, ORTG04NS
Primary DI / UDI-DI
10724995220966
FDA Product Code
NAB, GDY
GMDN Term
Radiopaque woven surgical sponge
Device Class
Class I
Regulation Number
878.4014, 878.4450
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Radiopaque woven surgical sponge

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No