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Cobb-XLR Excellerator™ CB-XLR1

by 5TH Interval Medical LLC

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860013965303 UDI-DI Date5 May 2025ListedStatusListed 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  • Withdrawn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
Cobb-XLR Excellerator™
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use
Model / Reference
CB-XLR1
Primary DI / UDI-DI
00860013965303
FDA Product Code
GCY
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use
Device Class
Class I
Regulation Number
878.4680
GUDID distribution status
In Commercial Distribution

Properties

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

Other properties (8)

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