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Onetrac™ Lxs C110200

by CooperSurgical, Inc.

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 Number00888937033823 UDI-DI Date10 Jul 2026ListedStatusListed 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  • Withdrawn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
Onetrac™ Lxs
Generic Name
Surgical/emergency suction cannula, illuminating, single-use
Model / Reference
C110200
Primary DI / UDI-DI
00888937033823
FDA Product Code
JOL
GMDN Term
Surgical/emergency suction cannula, illuminating, single-use
Device Class
Class II
Regulation Number
880.6740
GUDID distribution status
In Commercial Distribution

Other devices from CooperSurgical, Inc.

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Properties

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

Other properties (7)

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