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Ori Ds-100

by Operating Room Innovations, Inc.

Listed FDA GUDID listing, not in commercial distribution

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 Number06975424191464 UDI-DI Date4 Apr 2023ListedStatusListed GUDID: not 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  • Withdrawn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
Ori
Generic Name
Medical/surgical interventional tube/cable securement strap
Model / Ref / Catalog
DS-100
Primary DI / UDI-DI
06975424191464
FDA Product Code
PUI
GMDN Term
Medical/surgical interventional tube/cable securement strap
Device Class
Class II
Regulation Number
878.4370
GUDID distribution status
Not in Commercial Distribution

Other devices from Operating Room Innovations, Inc.

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No